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HS.txt
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> (-) NT_187502.1:1897-2180 Homo sapiens unplaced genomic scaffold, GRCh38.p7 Primary Assembly HSCHRUN_RANDOM_CTG24, NONE
GGGGTACTGTCACTCTGTTGCAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGT
GTAATCTGTCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTTGATGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCCTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGCCTCCTACAGATGCAGAGAGGGAGGATGGAGACTGGGTCATCTGGAT
GTCA
> (-) NT_187380.1:86010-86300 Homo sapiens chromosome 14 unlocalized genomic scaffold, GRCh38.p7 Primary Assembly HSCHR14_CTG7_UNLOCALIZED, ENSG00000237592
GGGAGGGGTACTGTCACTCTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTG
AGAGTGTAATCTGTCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGATGCAG
CATAGATCAGGAGCTTAGGAGTTTTCCCTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTG
ACTCGCCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATC
TGGATGTCACA
> (-) T1 NC_000002.12:94265056-94265338 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, NONE
GGGTACTGTCACTCTGTTGACAGTAATAAGCTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGT
GTAATCTGTCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGATGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCCTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGCCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (+) T1 NC_000002.12:91817962-91818230 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, LOC107985799, ENSG00000235235(PSEUDO)
GACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGGCAGAGTCACCATCACTTGCC
GGGCGAGTCAGGGCATTAGCAATAATTTAAATTGGTATCAGCAGAAACCAGGGAAAACTCCTAAGCTCCT
GATCTATGCTGCATCCAGTCTGCAAAGTGGGATTCCCTCTCGGTTCAGTGACAGTGGATCTGGGGCAGAT
TACACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAGCTTATTACTGTCAACA
> (-) T1 NC_000002.12:92034526-92034808 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, IGKV1OR2-2(PSEUDO), ENSG00000223816(PSEUDO)
GGGTACTGTCACTCTGTTGACAGTAATAAGCTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGT
GTAATCTGCCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGATGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCCTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGCCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (-) T1 NC_000002.12:90315370-90315652 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, IGKV1OR2-118 (PSEUDO), ENSG00000270999(PSEUDO)
GGGTACTGTCACTCTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCGGATGGTGAGAGT
GTAATCTGCCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGATGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCCTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (+) T1 NC_000002.12:91486973-91487255 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, NONE
GACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCC
GGGCGAGTCAGGGCATTAGCAATAATTTAAATTGGTATCAGCAGAAACCAGGGAAAACTCCTAAGCTCCT
GATCTATGCTGCACCCAGTCTGCAAAGTGGGATTCCCTCTCGGTTCAGTGACAGTGGATCTGGGGCAGAT
TACACTCTCACCATCCGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTACTGTCAACAGAGTGACAGTA
CCC
> (+) T1 NC_000002.12:89862695-89862977 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, IGKV1D-39, ENSG00000251546
GACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCC
GGGCAAGTCAGAGCATTAGCAGCTATTTAAATTGGTATCAGCAGAAACCAGGGAAAGCCCCTAAGCTCCT
GATCTATGCTGCATCCAGTTTGCAAAGTGGGGTCCCATCAAGGTTCAGTGGCAGTGGATCTGGGACAGAT
TTCACTCTCACCATCAGCAGTCTGCAACCTGAAGATTTTGCAACTTACTACTGTCAACAGAGTTACAGTA
CCC
> (-) T1 NC_000002.12:89319627-89319909 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, IGKV1-39, ENSG00000242371
GGGTACTGTAACTCTGTTGACAGTAGTAAGTTGCAAAATCTTCAGGTTGCAGACTGCTGATGGTGAGAGT
GAAATCTGTCCCAGATCCACTGCCACTGAACCTTGATGGGACCCCACTTTGCAAACTGGATGCAGCATAG
ATCAGGAGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAATTTAAATAGCTGCTAATGCTCTGACTTG
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (-) T1 NC_000002.12:89213425-89213707 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, IGKV1-27, ENSG00000244575
GGGCACTGTTATACTTTTGACAGTAATAAGTTGCAACATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGT
GAAATCTGTCCCAGATCCACTGCCACTGAACCGAGATGGGACCCCTGATTGCAAAGTGGATGCAGCATAG
ATCAGGAGCTTAGGAACTTTCCCTGGTTTCTGCTGATACCAGGCTAAATAATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (+) T1 NC_000002.12:89969059-89969338 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, IGKV1D-27(PSEUDO), ENSG00000224607(PSEUDO)
GACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCC
GGGCGAGTCAGGGCATTAGCAATTATTTAGCCTGGTATCAGCAGAAACCAGGGAAAGTTCCTAAGCTCCT
GATCTATGCTGCATCCGCTTTGCAATCAGGGGGTCCCATCTCGGTTCAGTGGCAGTGGATCTGGGACAGA
TTTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATGTTGCAACTTATTACTGTCAAAAGTATAACAGT
> (-) T1 NC_000002.12:89099860-89100143 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000240864, IGKV1D-16
GGGTAACTATTATACTGTTGGCAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAG
TGAAATCTGTCCCAGATCCACTGCCGCTGAACTTTGATGGGACCCCACTTTGCAAACTGGATGCAGCATA
GATCAGGGACTTAGGGGCTTTCCCTGGTTTCTGCTGAAACCAGGCTAAATAATTGCTAATGCCCTGACTC
GCCCGACAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGTGAGGATGGAGACTGGGTCATCTGGA
TGTC
> (-) T1 NC_000002.12:89117348-89117626 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000240382, IGKV1-17
ACTATTATGCTGTAGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATTGTGAGAGTGAAT
TCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTGCAAACTGGATGCAGCATAGATCA
GGCGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAGCCTAAATCATTTCTAATGCCCTGACTTGCCCG
GCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGATGTC
> (-) T1 NC_000002.12:89297266-89297548 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000239862, IGKV1-37
GGGCATTGTAAGTCCGTTGACCGTAATAAGTTGCAACATCTTCAGGCTGCAGGCTGCTGATAGTGAGAGT
GAAATCTGTCCCAGATCCACTGCCACTGAACCGAGATGGGACTCCAGATTGCAAATTGGATGCACTATAG
ATCAGGAGCTTAGGAACTTTCCCTGGTTTCTGCCGATACCAATTTAAATAACTGCTAATGCCCTGACTCA
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCAACTGGAT
GTC
> (+) T1 NC_000002.12:89884930-89885212 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000250036, IGKV1D-37
GACATCCAGTTGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCC
GGGTGAGTCAGGGCATTAGCAGTTATTTAAATTGGTATCGGCAGAAACCAGGGAAAGTTCCTAAGCTCCT
GATCTATAGTGCATCCAATTTGCAATCTGGAGTCCCATCTCGGTTCAGTGGCAGTGGATCTGGGACAGAT
TTCACTCTCACTATCAGCAGCCTGCAGCCTGAAGATGTTGCAACTTATTACGGTCAACGGACTTACAATG
CCC
> (-) T1 NC_000002.12:88966268-88966548 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000239855, IGKV1-6
ATTGTAATCTTGTAGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGTGAAA
TCTGTGCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTGTAAACTGGATGCAGCATAGATCA
GGAGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAGCCTAAATCATTTCTAATGCCCTGACTTGCCCG
GCAAGTGATGGTGACTCTGTCTCCAACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGATGGCA
C
> (+) T1 NC_000002.12:90154290-90154575 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000276566, IGKV1D-13
GCCATCCAGTTGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCC
GGGCAAGTCAGGGCATTAGCAGTGCTTTAGCCTGGTATCAGCAGAAACCAGGGAAAGCTCCTAAGCTCCT
GATCTATGATGCCTCCAGTTTGGAAAGTGGGGTCCCATCAAGGTTCAGCGGCAGTGGATCTGGGACAGAT
TTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTACTGTCAACAGTTTAATAGTT
ACCCTC
> (-) T1 NC_000002.12:89045990-89046272 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000253497(PSEUDO, IGKV1-13
AGGGTAATTATTAAACTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGA
GTGAAATCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTCCAAACTGGAGGCATCAT
AGATCAGGAGCTTAGGAGCTTTCCCTGGTTTCTGCTGATATCAGGCTAAAGCACTGCTAATGCCCTGACT
TGCCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCAACTGG
ATG
> (-) T1 NC_000002.12:89009980-89010266 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000241755, IGKV1-9
GGAGGGTAACTATTAAGCTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATTGTGA
GAGTGAATTCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTGCAAAGTGGATGCAGC
ATAGATCAGGAGCTTAGGGGCTTTCCCTGGTTTTTGCTGATACCAGGCTAAATAACTGCTAATGCCCTGA
CTGGCCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGAAGGATGGAGACTGGGTCAACT
GGATGTC
> (+) T1 NC_000002.12:90160051-90160335 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000278857, IGKV1D-12
GACATCCAGATGACCCAGTCTCCATCTTCCGTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGTC
GGGCGAGTCAGGGTATTAGCAGCTGGTTAGCCTGGTATCAGCAGAAACCAGGGAAAGCCCCTAAGCTCCT
GATCTATGCTGCATCCAGTTTGCAAAGTGGGGTCCCATCAAGGTTCAGCGGCAGTGGATCTGGGACAGAT
TTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAACTTACTATTGTCAACAGGCTAACAGTT
TCCCT
> (-) T1 NC_000002.12:89040225-89040508 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000243290, IGKV1-12
GGGAAACTGTTAGCCTGTTGACAATAGTAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAG
TGAAATCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTGCAAACTGGATGCAGCATA
GATCAGGAGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAGGCTAACCAGCTGCTAATACCCTGACTC
GCCCGACAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACACGGAAGATGGAGACTGGGTCATCTGGA
TGTC
> (-) T1 NC_000002.12:89268000-89268285 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000242076, IGKV1-33
GAGGGAGATTATCATACTGTTGACAGTAATATGTTGCAATATCTTCAGGCTGCAGGCTGCTGATGGTGAA
AGTAAAATCTGTCCCAGATCCACTTCCACTGAACCTTGATGGGACCCCTGTTTCCAAATTGGATGCATCG
TAGATCAGGAGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAATTTAAATAGTTGCTAATGTCCTGAC
TCGCCTGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTG
GATGTC
> (+) T1 NC_000002.12:89914261-89914545 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000239975, IGKV1D-33
GACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCC
AGGCGAGTCAGGACATTAGCAACTATTTAAATTGGTATCAGCAGAAACCAGGGAAAGCCCCTAAGCTCCT
GATCTACGATGCATCCAATTTGGAAACAGGGGTCCCATCAAGGTTCAGTGGAAGTGGATCTGGGACAGAT
TTTACTTTCACCATCAGCAGCCTGCAGCCTGAAGATATTGCAACATATTACTGTCAACAGTATGATAATC
TCCCT
> (+) T1 NC_000002.12:90100454-90100735 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000241244, IGKV1D-16
GACATCCAGATGACCCAGTCTCCATCCTCACTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGTC
GGGCGAGTCAGGGTATTAGCAGCTGGTTAGCCTGGTATCAGCAGAAACCAGAGAAAGCCCCTAAGTCCCT
GATCTATGCTGCATCCAGTTTGCAAAGTGGGGTCCCATCAAGGTTCAGCGGCAGTGGATCTGGGACAGAT
TTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTACTGCCAACAGTATAATAGTT
AC
> (+) T1 NC_000002.12:90083008-90083290 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000242766, IGKV1D-17
ACATCCAGATGACCCAGTCTCCATCTGCCATGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGTCG
GGCGAGGCAGGGCATTAGCAATTATTTAGCCTGGTTTCAGCAGAAACCAGGGAAAGTCCCTAAGCACCTG
ATCTATGCTGCATCCAGTTTGCAAAGTGGGGTCCCATCAAGGTTCAGCGGCAGTGGATCTGGGACAGAAT
TCACTCTCACAATCAGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTACTGTCTACAGCATAATAGTTA
CCC
> (-) T1 NC_000002.12:88992436-88992718 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000240671, IGKV1-8
ATAAGTTGCAAAATCTTCAGACTGCAGGCAGCTGATGGTGAGAGTGAAATCTGTCCCAGATCCACTGCCG
CTGAACCTTGATGGGACCCCACTTTGCAAAGTGGATGCAGCATAGATCAGGAGCTTAGGGGCTTTCCCTG
GTTTTTGCTGATACCAGGCTAAATAACTGCTAATACCCTGACTCGCCCGACAAGTGATGGTGACTCTGTC
TCCTGTAGATGCAGAGAATGAGGATGGAGACTGGGTCATCCGGATGGCACATCTGGCACCTGAGATTGGA
AAC
> (+) T1 NC_000002.12:113406586-113406868 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000231292, IGKV1OR2-108
GACATCCAGGTGACCCAGTCTCCATCTTCCCTGTCTGCGTCTGTAGGAGACAGAGTCACCATCACCTGCC
GGGCAAGTCAGGGCATTAGCAATGGGTTATCCTGGTATCAGCAGAAACCAGGGCAAGCCCCTACGCTCCT
GATCTATGCTGCATCCAGTTTGCAGTCGGGGGTCCCATCTCGGTTCAGTGGCAGTGGATCTGGGACAGAT
TTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATGTTGCAACTTATTACTGTCTACAGGATTATACTA
CCC
> (+) T1 NC_000002.12:90210245-90210527 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000242580, IGKV1D-43
GCCATCCGGATGACCCAGTCTCCATTCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCT
GGGCCAGTCAGGGCATTAGCAGTTATTTAGCCTGGTATCAGCAAAAACCAGCAAAAGCCCCTAAGCTCTT
CATCTATTATGCATCCAGTTTGCAAAGTGGGGTCCCATCAAGGTTCAGCGGCAGTGGATCTGGGACGGAT
TACACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTACTGTCAACAGTATTATAGTA
CCC
> (+) T1 NC_000002.12:90221100-90221382 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000239819, IGKV1D-8
CATCTGGATGACCCAGTCTCCATCCTTACTCTCTGCATCTACAGGAGACAGAGTCACCATCAGTTGTCGG
ATGAGTCAGGGCATTAGCAGTTATTTAGCCTGGTATCAGCAAAAACCAGGGAAAGCCCCTGAGCTCCTGA
TCTATGCTGCATCCACTTTGCAAAGTGGGGTCCCATCAAGGTTCAGTGGCAGTGGATCTGGGACAGATTT
CACTCTCACCATCAGCTGCCTGCAGTCTGAAGATTTTGCAACTTATTACTGTCAACAGTATTATAGTTTC
CCT
> (+) T1 NC_000002.12:97355059-97355341 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000271569(PSEUDO), IGKV1OR2-6
GCCATCCAGATGACCCAGCCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGTGTCACCATCACTTGCC
GGGCGAGTCAGAGTTTTACCAATCAGTTAGCCTGGTATCAGCAGAAACCAGGGAAAGCTCCTAAGCTCCT
GATATATAGGGTATCCAGTTTGCAAACGGGGGTTCCATCTCTGTTCAGTGGTAGTGAATCTGGGACAGAT
TTCACTCTAACCATCAGCAGCCTGCAGCCTGATGATGTTGCAACTTACTACTGTCAACAGTAACTCCCAC
AGT
> (+) T1 NC_000002.12:89895504-89895786 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000232747(PSEUDO), IGKV1D-35
GACATCCAGTCACCCAGTCTCCATCCACACTGTCTGCATCTGTAAGGAGACAGCGTCACCATCACTTGCC
GGGCGAGTCAGAGCATTGGTAGTAATTTAGACTGGTATCAGCAGAAACCAGGGAAGGCCCCTAAGGGCCT
GATCTATGCTGCATCCAGTTTGCAATCTGGGGCTCCTTCGCGGTTCGGTGGCAGTGGATCTGGGACAGAT
TTTACTCTCACCATCAGAATCCTGCAGCCTAAAGATGTTGCAACTTATTACTGTCAACAGTATAAAAATT
ACC
> (-) T1 NC_000002.12:89286695-89286980 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000253461(PSEUDO), IGKV1-35
TAGGGTAATTTTTATACTGTTGACAGTAATAAGTTGCAACATCTTTAGGCTGCAGGATTCTGATGGTGAG
AGTAAAATCTGTCCCAGATCCACTGCCACCGAACCGCGAAGGAGCCCCAGATTGCAAACTGGATGCAGCA
TAGATCAGGCCCTTAGGGGCCTTCCCTGGTTTCTGCTGATACCAGTCTAAATTACTACCAATGCTCTGAC
TCGCCCGGCAAGTGATGGTGACACTGTCTCCTTACAGATGCAGACAGTGTGGATGGAGACTGGGTGACTG
GATGTC
> (+) T1 NC_000002.12:97060129-97060413 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000204670(PSEUDO), IGKV1OR2-3
GACATCCAGATGACCCAGCCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCGTCTCTTGCC
AGGCTAGTCAAAGCATTTACAACTATTTAAATTGGTATCAGCAGAAACCAGGGAAAGCACCTAAGTTCCT
GACCTATAGGGCATCCAGTTTGCAGAGGGGGATGCCATCTCAGTTCAGTGGCAGCGGATATGGAAGAGAT
TTCACTCTCACTGTCAGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTAATGTCAACAAGAGAGCATTT
TCCCT
> (-) T1 NC_000002.12:88947300-88947585 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000243466, IGKV1-5
GAGAATAACTATTATACTGTTGGCAGTAATAAGTTGCAAAATCATCAGGCTGCAGGCTGCTGATGGTGAG
AGTGAATTCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTCTAAACTAGACGCCTTA
TAGATCAGGAGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAGGCCAACCAGCTACTAATACTCTGAC
TGGCCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGTGGAAGGAGACTGGGTCATCTG
GATGTC
> (-) T1 NC_000002.12:97322140-97322423 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000271351(PSEUDO), IGKV1OR2-9
GGGAAAATGCTCTCTTGTTGACATTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGACGGTGAGAG
TGAAATCTCTTCCATATCCGCTGCCACTGAACTGAGATGGCATCGCCCTCTGCAAACTGGATGCCCTATA
GGTCAGGAACTTAGGTGCTTTCCCTGGTTTCTGCTGATACCAATTTAAATAGTTGTAAATGCTTTGACTA
GCCTGGCAAGAGACGGTGGCTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGGCTGAGTCATCTGGA
TGTC
> (+) T1 NC_000002.12:97386082-97386365 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000270187(PSEUDO), IGKV1OR2-11
GACATCCAGATGACTCAGCCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGCCACCGTCTCTTGCC
AGGCTAGTCAAAGCATTTACAACTATTTAAATTGGTATCAGCAGAAACCAGGGAAAGCACCTAAGTTCCT
GACCTATAGGGCATCCAGTTTGCAGAGGGCGATGCCATCTCAGTTCAGTGGCAGCGGATATGGAAGAGAT
TTCACTCTCACCGTCAGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTAATGTCAACAAGAGAGCATTT
TCCC
> (-) T1 NC_000002.12:90010920-90011206 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000253365(PSEUDO), IGKV1D-22
GATTTCCAGATGACTCAGTCTCCATCCTCCCTGACTGCATCTGTAGGAGAGAGAGTCACCATCACTTGCT
GGGCGAGTCAGGGCATTTGCAATTATTTAAGCTAGTATCAGTAGAAACTAGAGAATCCTCCTAAGCTCCT
GATCTATGCTGCATCCAGTTTGCAATCTGGGGTCCCGTCACGGTTCAGTGGCAGTAGGTCTGGGACACAT
TTCACACATTCTCACCATCAGGAGCCTGCAACCTGAAGATGTTATAACTTATTACTGTCTATAGACTTAC
AGCAGCC
> (+) T1 NC_000002.12:90190395-90190676 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000211633, IGKV1D-42
GACATCCAGATGACCCAGTCTCCATCTTTCCTGTCTGCATCTGTAGGAGACAGAGTCAGTATCATTTGCT
GGGCAAGTGAGGGCATTAGCAGTAATTTAGCCTGGTATCTGCAGAAACCAGGGAAATCCCCTAAGCTCTT
CCTCTATGATGCAAAAGATTTGCACCCTGGGGTCTCATCGAGGTTCAGTGGCAGGGGATCTGGGACGGAT
TTCACTCTCACCATCATCAGCCTGAAGCCTGAAGATTTTGCAGCTTATTACTGTAAACAGGACTTCAGTT
AC
> (-) T1 NC_000002.12:89085180-89085461 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000244437, IGKV3-15
CCAGTTATTATACTGCTGACAGTAATAAACTGCAAAATCTTCAGACTGCAGGCTGCTGATGGTGAGAGTG
AACTCTGTCCCAGACCCACTGCCACTGAACCTGGCTGGGATACCAGTGGCCCTGGTGGATGCACCATAGA
TGAGGAGCCTGGGAGCCTGGCCAGGTTTCTGCTGGTACCAGGCTAAGTTGCTGCTAACACTCTGACTGGC
CCTGCAGGAGAGGGTGGCTCTTTCCCCTGGAGACACAGACAGGGTGGCTGGAGACTGCGTCATCACTATT
TC
> (+) T1 NC_000002.12:90115116-90115397 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000224041, IGKV3D-15
GAAATAGTGATGACGCAGTCTCCAGCCACCCTGTCTGTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCA
GGGCCAGTCAGAGTGTTAGCAGCAACTTAGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAGGCTCCT
CATCTATGGTGCATCCATCAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACAGAG
TTCACTCTCACCATCAGCATCCTGCAGTCTGAAGATTTTGCAGTTTATTACTGTCAGCAGTATAATAACT
GG
> (+) T1 NC_000002.12:87338746-87339030 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, LOC100652743(PSEUDO), ENSG00000233999, IGKV3OR2-268
GAAATTGTAATGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCA
GGGCCAGTCAGAGTGTTAGCAGCAGCTACTTATCCTGGTACCAGCAGAAACCTGGGCAGGCTCCCAGGCT
CCTCATCTATGGTGCATCCACCAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACA
GACTTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAGTTTATTACTGTCAGCAGGATTATA
ACTTA
> (+) T1 NC_000002.12:90235081-90235365 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, IGKV3D-7, ENSG00000228325
GAAATTGTAATGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCA
GGGCCAGTCAGAGTGTTAGCAGCAGCTACTTATCCTGGTACCAGCAGAAACCTGGGCAGGCTCCCAGGCT
CCTCATCTATGGTGCATCCACCAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACA
GACTTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAGTTTATTACTGTCAGCAGGATTATA
ACTTA
> (-) T1 NC_000002.12:88978471-88978755 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000243063, IGKV3-7
TAAGTTATAATCCTGCTGACAGTAATAAACTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGTG
AAGTCTGTCCCAGACCCACTGCCACTGAACCTGGCTGGGATGCTAGTGGCCCTGGTGGATGCACCATAGA
TGAGGAGCCTGGGCGCCTGGCCAGGTTTCTGCTGATACCAGGTTAAGTAGCTGCTGCTAACACTCTGACT
GGCCCTGCAGGAGAGGGTGACTCTTTCCCCTGGAGACAAAGACAGGGTGGGTGGAGACTGTGTCATTACA
ATTTC
> (-) T1 NC_000002.12:89253550-89253831 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000253870(PSEUDO), IGKV1-32
TTTATACTGTTGACCAATAATAAGAAGTTGCAGCAACTTCAGACTGGAGGATGCTAATGGTGAGAATCAA
ATCTGTCCTGGATCCAATGCCACATAACTGCAATGGGACCCAGGTTTGCAAATTGGATGCATCGTAGATC
AGGAGCTCAGAAGCTTTCCCTGGCTTCTCTTTGTATCAGGCTAAAACATGGCTAATGCCCTGCCTGACTT
TCCTGGCATGTGATGGTGACTCTCACCTAGACAGGAAGACAGCGAGGATGGAGACTGGGTCATCTGCATG
TC
> (+) T1 NC_000002.12:89928606-89928890 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000253191(PSEUDO), IGKV1D-32
GACATGCAGATGACCCAGTCTCCATCCTCGCTGTCTTCCTGTCTAGGTGAGAGTCACCATCACATGCCAG
GAAAGTCAGGTAGGGCATTAGCCATGTTTTAGCCTGATACAAAGAGAAGCCAGGGAAAGCTTCTGAGCTC
CTGATCTACGATGCATCCAATTTGCAAACCTGGGTCCCATTGCAGTTATGTGGCATTGGATCCAGGACAG
ATTTGATTCTCACCATTAGCATCCTCCAGTCTGAAGTTGCTGCAACTTCTTATTATTGGTCAACAGTATA
AAAGT
> (-) T1 NC_000002.12:89027173-89027455 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000241351, IGKV3-11
GCCAGTTGCTACGCTGCTGACAGTAATAAACTGCAAAATCTTCAGGCTCTAGGCTGCTGATGGTGAGAGT
GAAGTCTGTCCCAGACCCACTGCCACTGAACCTGGCTGGGATGCCAGTGGCCCTGTTGGATGCATCATAG
ATGAGGAGCCTGGGAGCCTGGCCAGGTTTCTGTTGGTACCAGGCTAAGTAGCTGCTAACACTCTGACTGG
CCCTGCAGGAGAGGGTGGCTCTTTCCCCTGGAGACAAAGACAGGGTGGCTGGAGACTGTGTCAACACAAT
TTC
> (-) T1 NC_000002.12:89159754-89160035 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000211611, IGKV6-21
TAAACTACTACTCTGATGACAGTAATACGTTGCAGCATCTTCAGCTTCCAGGCTATTGATGGTGAGGGTG
AAATCTGTCCCAGATCCACTGCCACTGAACCTCGAGGGGACCCCTGAGAAGGACTGGGAAGCATACTTGA
TGAGGAGCTTTGGAGACTGATCTGGTTTCTGCTGGTACCAGTGTAAGCTACTACCAATGCTCTGACTGGC
CCGGCAGGTGATGGTGACTTTCTCCTTTGGAGTCACAGACTGAAAGTCTGGAGACTGAGTCAGCACAATT
TC
> (+) T1 NC_000002.12:90069954-90070235 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000211626, IGKV6D-41
GATGTTGTGATGACACAGTCTCCAGCTTTCCTCTCTGTGACTCCAGGGGAGAAAGTCACCATCACCTGCC
AGGCCAGTGAAGGCATTGGCAACTACTTATACTGGTACCAGCAGAAACCAGATCAAGCCCCAAAGCTCCT
CATCAAGTATGCTTCCCAGTCCATCTCAGGGGTCCCCTCGAGGTTCAGTGGCAGTGGATCTGGGACAGAT
TTCACCTTTACCATCAGTAGCCTGGAAGCTGAAGATGCTGCAACATATTACTGTCAGCAGGGCAATAAGC
AC
> (+) T1 NC_000002.12:90173128-90173411 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000211632, IGKV3D-11
GAAATTGTGTTGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCA
GGGCCAGTCAGAGTGTTAGCAGCTACTTAGCCTGGTACCAGCAGAAACCTGGCCAGGCTCCCAGGCTCCT
CATCTATGATGCATCCAACAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGCCTGGGACAGAC
TTCACTCTCACCATCAGCAGCCTAGAGCCTGAAGATTTTGCAGTTTATTACTGTCAGCAGCGTAGCAACT
GGCA
> (+) T1 NC_000002.12:90021901-90022182 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000225523, IGKV6D-21
GAAATTGTGCTGACTCAGTCTCCAGACTTTCAGTCTGTGACTCCAAAGGAGAAAGTCACCATCACCTGCC
GGGCCAGTCAGAGCATTGGTAGTAGCTTACACTGGTACCAGCAGAAACCAGATCAGTCTCCAAAGCTCCT
CATCAAGTATGCTTCCCAGTCCATCTCAGGGGTCCCCTCGAGGTTCAGTGGCAGTGGATCTGGGACAGAT
TTCACCCTCACCATCAATAGCCTGGAAGCTGAAGATGCTGCAGCGTATTACTGTCATCAGAGTAGTAGTT
TA
> (-) T1 NC_000002.12:89142578-89142861 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000239951, IGKV3-20
GAGCTACCATACTGCTGACAGTAATACACTGCAAAATCTTCAGGCTCCAGTCTGCTGATGGTGAGAGTGA
AGTCTGTCCCAGACCCACTGCCACTGAACCTGTCTGGGATGCCAGTGGCCCTGCTGGATGCACCATAGAT
GAGGAGCCTGGGAGCCTGGCCAGGTTTCTGCTGGTACCAGGCTAAGTAGCTGCTGCTAACACTCTGACTG
GCCCTGCAGGAGAGGGTGGCTCTTTCCCCTGGAGACAAAGACAGGGTGCCTGGAGACTGCGTCAACACAA
TTTC
> (-) T1 NC_000002.12:89176331-89176627 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000241294, IGKV2-24
AAATTGTGTAGCTTGCATGCAGTAATAAACCCCGACATCCTCAGCTTCCACCCTGCTGATTTTCAGTGTG
AAATCTGTCCCTGCCCCACTGCCACTGAATCTGTCTGGGACCCCAGAGAACCGGTTAGAAATCTTATAAA
TTAGGAGTCTTGGAGGCTGGCCTGGCCTCTGCTGAAGCCAACTCAAGTAGGTGTTTCCATCACTGTGTAC
GAGGCTTTGACTAGACCTGCAGGAGATGGAGGCCGGCTGTCCAAGGGTGACAGGTGAGGAGAGTGGAGTC
TGGGTCATCACAATATC
> (+) T1 NC_000002.12:90005330-90005626 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000241566, IGKV2D-24
GATATTGTGATGACCCAGACTCCACTCTCCTCGCCTGTCACCCTTGGACAGCCGGCCTCCATCTCCTTCA
GGTCTAGTCAAAGCCTCGTACACAGTGATGGAAACACCTACTTGAGTTGGCTTCAGCAGAGGCCAGGCCA
GCCTCCAAGACTCCTAATTTATAAGGTTTCTAACCGGTTCTCTGGGGTCCCAGACAGATTCAGTGGCAGT
GGGGCAGGGACAGATTTCACACTGAAAATCAGCAGGGTGGAAGCTGAGGATGTCGGGGTTTATTACTGCA
CGCAAGCTACACAATTT
> (+) T1 NC_000002.12:90039192-90039476 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000211625, IGKV3D-20
GAAATTGTGTTGACGCAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCG
GGGCCAGTCAGAGTGTTAGCAGCAGCTACTTAGCCTGGTACCAGCAGAAACCTGGCCTGGCGCCCAGGCT
CCTCATCTATGATGCATCCAGCAGGGCCACTGGCATCCCAGACAGGTTCAGTGGCAGTGGGTCTGGGACA
GACTTCACTCTCACCATCAGCAGACTGGAGCCTGAAGATTTTGCAGTGTATTACTGTCAGCAGTATGGTA
GCTCA
> (-) T1 NC_000002.12:89221700-89221997 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000244116, IGKV2-28
GAGTTTGTAGAGCTTGCATGCAGTAATAAACCCCAACATCCTCAGCCTCCACTCTGCTGATTTTCAGTGT
AAAATCTGTGCCTGATCCACTGCCACTGAACCTGTCAGGGACCCCGGAGGCCCGATTAGAACCCAAATAG
ATCAGGAGCTGTGGAGACTGCCCTGGCTTCTGCAGGTACCAATCCAAATAGTTGTATCCATTACTATGCA
GGAGGCTCTGACTAGACCTGCAGGAGATGGAGGCCGGCTCTCCAGGGGTGACGGGCAGGGAGAGTGGAGA
CTGAGTCATCACAATATC
> (+) T1 NC_000002.12:89960449-89960745 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000242534, IGKV2D-28
GATATTGTGATGACTCAGTCTCCACTCTCCCTGCCCGTCACCCCTGGAGAGCCGGCCTCCATCTCCTGCA
GGTCTAGTCAGAGCCTCCTGCATAGTAATGGATACAACTATTTGGATTGGTACCTGCAGAAGCCAGGGCA
GTCTCCACAGCTCCTGATCTATTTGGGTTCTAATCGGGCCTCCGGGGTCCCTGACAGGTTCAGTGGCAGT
GGATCAGGCACAGATTTTACACTGAAAATCAGCAGAGTGGAGGCTGAGGATGTTGGGGTTTATTACTGCA
TGCAAGCTCTACAAACT
> (+) T1 NC_000002.12:89986403-89986699 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000211623, IGKV2D-26
GAGATTGTGATGACCCAGACTCCACTCTCCTTGTCTATCACCCCTGGAGAGCAGGCCTCCATGTCCTGCA
GGTCTAGTCAGAGCCTCCTGCATAGTGATGGATACACCTATTTGTATTGGTTTCTGCAGAAAGCCAGGCC
AGTCTCCACGCTCCTGATCTATGAAGTTTCCAACCGGTTCTCTGGAGTGCCAGATAGGTTCAGTGGCAGC
GGGTCAGGGACAGATTTCACACTGAAAATCAGCCGGGTGGAGGCTGAGGATTTTGGAGTTTATTACTGCA
TGCAAGATGCACAAGAT
> (-) T1 NC_000002.12:89330119-89330418 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000273962, IGKV2-40
AAACTCTATACGTTGCATGCAGTAATAAACTCCAACATCCTCAGCCTCCACCCTGCTGATTTTCAGTGTG
AAATCAGTGCCTGACCCACTGCCACTGAACCTGTCTGGGACTCCAGAGGCCCGATAGGAAAGCGTATAGA
TCAGGAGCTGTGGAGACTGCCCTGGCTTCTGCAGGTACCAGTCCAAATAGGTGTTTCCATCATCACTATC
CAAGAGGCTCTGACTAGACCTGCAGGAGATGGAGGCCGGCTCTCCAGGGGTGACGGGCAGGGAGAGTGGA
GTCTGGGTCATCACAATATC
> (+) T1 NC_000002.12:89852189-89852488 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000251039, IGKV2D-40
GATATTGTGATGACCCAGACTCCACTCTCCCTGCCCGTCACCCCTGGAGAGCCGGCCTCCATCTCCTGCA
GGTCTAGTCAGAGCCTCTTGGATAGTGATGATGGAAACACCTATTTGGACTGGTACCTGCAGAAGCCAGG
GCAGTCTCCACAGCTCCTGATCTATACGCTTTCCTATCGGGCCTCTGGAGTCCCAGACAGGTTCAGTGGC
AGTGGGTCAGGCACTGATTTCACACTGAAAATCAGCAGGGTGGAGGCTGAGGATGTTGGAGTTTATTACT
GCATGCAACGTATAGAGTTT
> (+) T1 NC_000002.12:97050729-97051025 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000271402(PSEUDO), IGKV2OR2-2, LOC107985918
GATATTGTGATCGCCCAGACTCCACTCTCCTGGCCTGTCACCTCTGGAGAGCTACCCACATATCCTGTAG
GTCTAGTCAGAGCCTCTTGTCCAGTGATGGATACACCTATTCGTATTGGTTCCTGCAGAAGCCAGGCCAG
TCTCCACAGCTCCTGATCTATTTTGTTTCAAACCGGGCCTCTGGAGTCCCAGACAGGTTCAATGGCAGTG
GGTCAGGCACTGATTTCACACTGAAAATCAGCCGGGTGGAGCTGAAGATGTTGGGGTTTATTACTGCATG
CAGGCTCTGCAGCTTCC
> (+) T1 NC_000002.12:97376674-97376968 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000278537(PSEUDO), IGKV2OR2-8, IGKV2OR2-10
GATACTGTGATGGCCCAGACTCCACTCTCCTGGCCTGTCGCCTCTAGAGAGCCACCCCCATATCCTGTAG
GTCTAGTCAGAGCCTCTTGTCCAGTGATGGATACACCTATTCGTATTGGTTCCTGCAGAAGCCAGGCCAG
TCTCCACAGCTCCTGATCTATTTTGTTTCAAACCGGGCCTCTGGAGTCCCAGACAGGTTCAATGGCAGTG
GGTCAGGCACTGATTTCACACTGAAAATCAGCCGGGTGGAGCTGAAGATGTTGGGGTTTATTACTGCATG
CAGGCTCTGCAGCTT
> (-) T1 NC_000002.12:97331538-97331832 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000276050(PSEUDO), IGKV2OR2-10, IGKV2OR2-8
AAGCTGCAGAGCCTGCATGCAGTAATAAACCCCAACATCTTCAGCTCCACCCGGCTGATTTTCAGTGTGA
AATCAGTGCCTGACCCACTGCCATTGAACCTGTCTGGGACTCCAGAGGCCCGGTTTGAAACAAAATAGAT
CAGGAGCTGTGGAGACTGGCCTGGCTTCTGCAGGAACCAATACGAATAGGTGTATCCATCACTGGACAAG
AGGCTCTGACTAGACCTACAGGATATGGGGGTGGCTCTCTAGAGGCGACAGGCCAGGAGAGTGGAGTCTG
GGCCATCACAGTATC
> (+) T1 NC_000002.12:88885851-88886150 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000211598, IGKV4-1
GACATCGTGATGACCCAGTCTCCAGACTCCCTGGCTGTGTCTCTGGGCGAGAGGGCCACCATCAACTGCA
AGTCCAGCCAGAGTGTTTTATACAGCTCCAACAATAAGAACTACTTAGCTTGGTACCAGCAGAAACCAGG
ACAGCCTCCTAAGCTGCTCATTTACTGGGCATCTACCCGGGAATCCGGGGTCCCTGACCGATTCAGTGGC
AGCGGGTCTGGGACAGATTTCACTCTCACCATCAGCAGCCTGCAGGCTGAAGATGTGGCAGTTTATTACT
GTCAGCAATATTATAGTACT
> (-) T1 NC_000002.12:89234185-89234484 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000253998(PSEUDO), IGKV2-29
AGGAAGGTGTATACCTTGCATTCAGTAATAAACCCCAACATCCTCAGCCTCCACCCGGCTGATTTTCAGT
GTGAAATCTGTCCCTGACCCGCTGCCACTGAACCTATCTGGCACTCCAGAGAACCGGCTGGAAACTTCAT
AGATCAGGAGCTGTGGAGACTGGCCTGGCTTCTGCAGGTACCAATACAAATAGGTCTTTCCATCACTATG
CAGGAGGCTCTGACTAGACTTGCAGGAGATGGAGGCCGGCTGTCCAGGGGTGACGGACAGAGAGAGTGGA
GTCTGGGTCATCACAATATC
> (+) T1 NC_000002.12:89947970-89948266 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000243264, IGKV2D-29
GATATTGTGATGACCCAGACTCCACTCTCTCTGTCCGTCACCCCTGGACAGCCGGCCTCCATCTCCTGCA
AGTCTAGTCAGAGCCTCCTGCATAGTGATGGAAAGACCTATTTGTATTGGTACCTGCAGAAGCCAGGCCA
GCCTCCACAGCTCCTGATCTATGAAGTTTCCAACCGGTTCTCTGGAGTGCCAGATAGGTTCAGTGGCAGC
GGGTCAGGGACAGATTTCACACTGAAAATCAGCCGGGTGGAGGCTGAGGATGTTGGGGTTTATTACTGCA
TGCAAAGTATACAGCTT
> (-) T1 NC_000002.12:88915080-88915376 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000197794(PSEUDO),IGKV7-3
AGGAAAATTCTTACTCTGCAGACAGTAATAATTTGCAGTATCATTAGCTTCCACAGGATTAATTGTGAGG
GTGAAATCGGTCCCAGACCCACTGCCGCTGAACCTGGCTGGGACCCCAGTGTCTTTATTGGATGCTTGGT
AAATCAGGAGTTTAGGAGGTTGTCCTGGTTTCTGCTGATACCAGTGAATTAAGTTTATTCCCAAGAAACT
GACACTCTCACTGGCTCTGCAGGTGATGGTGGCCCTCTGTCCTGGAGACACGGCCAAGGAGGCTGGAGAC
TGGGTCAGCACAATGTC
> (+) T1 NC_000002.12:90053059-90053355 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000254220, IGKV2D-18
GATATTGTGATGACCCAGACTCCACCCTCCCTGCCCGTCAACCCTGGAGAGCCGGCCTCCATCTCCTGCA
GGTCTAGTCAAAGCCTCCTGCATAGTAATGGATATACCTATTTGCATTGGTACCCGCAGAAGCCAGGGCA
ATCTCCACAGCTCCTGATTTATAGGGTTTCCAGTCGTTTTTCTGGGGTCCCAGACAGGTTTAGTGGCAGT
GGGTCAGGCAGTGATTTCACACTGAAAATCAGCTGGGTGGAGGCTGAGGATGTTGGGGTTTATTACTGCA
TGCAAGCTACACAGTTT
> (-) T1 NC_000002.12:89244803-89245080 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000243238, IGKV2-30
CAGTAATAAACCCCAACATCCTCAGCCTCCACCCTGCTGATTTTCAGTGTGAAATCAGTGCCTGACCCAC
TGCCGCTGAATCTGTCTGGGACCCCAGAGTCCCGGTTAGAAACCTTATAAATTAGGCGCCTTGGAGATTG
GCCTGGCCTCTGCTGAAACCAATTCAAGTAGGTGTTTCCATCACTGTATACGAGGCTTTGACTAGACCTG
CAGGAGATGGAGGCCGGCTGTCCAAGGGTGACGGGCAGGGAGAGTGGAGACTGAGTCATCACAACATC
> (+) T1 NC_000002.12:89937380-89937676 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000239571, IGKV2D-30
GATGTTGTGATGACTCAGTCTCCACTCTCCCTGCCCGTCACCCTTGGACAGCCGGCCTCCATCTCCTGCA
GGTCTAGTCAAAGCCTCGTATACAGTGATGGAAACACCTACTTGAATTGGTTTCAGCAGAGGCCAGGCCA
ATCTCCAAGGCGCCTAATTTATAAGGTTTCTAACTGGGACTCTGGGGTCCCAGACAGATTCAGCGGCAGT
GGGTCAGGCACTGATTTCACACTGAAAATCAGCAGGGTGGAGGCTGAGGATGTTGGGGTTTATTACTGCA
TGCAAGGTACACACTGG
> (+) T1 NC_000002.12:89929957-89930236 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000253999(PSEUDO), IGKV3D-31
GAACTTGTGATGACAGTCTCCAGCCTCCCTGTCTTTATCTCTAGGGGAAAAAGCCACCCTCACCTACAGA
GCCAAGTAGACTATTAGCAGCTCCTTAGCAGGGTATCAGTGGAAACCTGGACAGGCTCTCAGGCTCCTCA
TCCATGGTGCATCCACCAGGACCACCAATGTCCCAGCCTGGTGGAGTGGCAGTGGGTTCGGGGAAAACTT
CAGTCTCATTATCAGCAGGCTGGAGCATGAAGATTTTGCACTTTAACACTGTTATCAGCATAGTGGTGGG
> (-) T1 NC_000002.12:89252200-89252480 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000253158, IGKV3-31
ACCCACCACTATGCTGATAACAGTGTTAAAGTGCAAAATCTTCATGCTCCAGCCTGCTGATAATGAGACT
GAAGTTTTCCCCGAACCCACTGCCACTCCACCAGGCTGGGACATTGGTGGTCCTGGTGGATGCACCATGG
ATGAGGAGCCTGAGAGCCTGTCCAGGTTTCCACTGATACCCTGCTAAGGAGCTGCTAATAGTCTACTTGG
CTCTGTAGGTGAGGGTGGCTTTTTCCCCTAGAGATAAAGACAGGGAGGCTGGAGACTGTCATCACAAGTT
C
> (+) T1 NC_000002.12:88897500-88897781 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000211599, IGKV5-2
GAAACGACACTCACGCAGTCTCCAGCATTCATGTCAGCGACTCCAGGAGACAAAGTCAACATCTCCTGCA
AAGCCAGCCAAGACATTGATGATGATATGAACTGGTACCAACAGAAACCAGGAGAAGCTGCTATTTTCAT
TATTCAAGAAGCTACTACTCTCGTTCCTGGAATCCCACCTCGATTCAGTGGCAGCGGGTATGGAACAGAT
TTTACCCTCACAATTAATAACATAGAATCTGAGGATGCTGCATATTACTTCTGTCTACAACATGATAATT
TC
> (-) T1 NC_000002.12:89309902-89310205 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000253592(PSEUDO), IGKV2-38
AAGGATATTATGTAGCTTGCATGTATTAATAAAGTCGAATATCCTCAGCCTCCACCCTGCTAATTTTGAG
TTTAAAATATGTGCCTGACCCACTGCTATTGAACCTGTCTGGGACTCCAGAGGCCCCATTGGAAACCCCA
TAGATCAGGAGCTGTGGAGACTCGCCTGGCTTCTATAGTTACCAATACAAATAGGTGTTTCCATTGCTAT
GCAGGAGGGTCTGACTAGACCTGCAGGAGATGAAGTACAAAGTTATGTACAAATATTATGAGCAAGTATC
ACGATTTCCCTTATGATATGGATT
> (+) T1 NC_000002.12:89872455-89872700 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000254009(PSEUDO), IGKV2D-38
TGTACTTCATCTCCTGCAGGTCTAGTCAGACCCTCCTGCATAGCAATGGAAACACCTATTTGTATTGGTA
ACTATAGAAGCCAGGCGAGTCTCCACAGCTCCTGATCTATGGGGTTTCCAATGGGGCCTCTGGAGTCCCA
GACAGGTTCAATAGCAGTGGGTCAGGCACATATTTTAAACTCAAAATTAGCAGGGTGGAGGCTGAGGATA
TTCGACTTTATTAATACATGCAAGCTACATAATATC
> (-) T1 NC_000002.12:89128710-89129005 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000254157(PSEUDO), IGKV2-18
AACTGTGTAGCTTGCATGCAGTAATAAACCCCAACATCCTCAGCCTCCACCCAGCTGATTTTCAGTGTGA
AATCACTACCTGACCCACTGCCACTAAACCTGTCTGGGACCCCAGAAAGATGATTGGAAACCCTATAAAT
CAGGAGCTGTGGAGACTGCCCTGGCTTCTGCAGGTACCAATGCAAATAGGTATATCCATTACTATGCAGG
AGGCTCTGACTAGACCTGCAAGAGATGGAGGCCGGCTCTCCAGGGTTGACGGGCAGGGAGGGTGGAGTCT
GGGTCATCACAATATC
> (+) T1 NC_000002.12:89990000-89990253 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000254097(PSEUDO), IGKV3D-25
GAAACAGTGATGACACAGTCTCCAGCTTCCCTGTCTTTGTCTCTGGAGAAAAAAGCCACCCTGACTTGCA
GGGCCAGTCAGTGTTAGCAGCTACTAAGCCTGGTACCAGAAGAAACCTGAGCGGGCTCCCAGGCTCCTCA
TCTATGGTACAGCCCTGATTTGTGATAGTGGGTCAGGACAGGGCTTACTCTCACCATCGGCAGGCTGGAG
CCTGAAGATTTGCACTTCATCACTGTTATCAGCATAGTAGTTGG
> (-) T1 NC_000002.12:89192495-89192757 Homo sapiens chromosome 2, GRCh38.p7 Primary Assembly, ENSG00000253202(PSEUDO), IGKV3-25
ACCAACTACTATGCTGATAACAGTGATGAAGTGCAAATCTCCAGGCTCCAGGCTCCAGGCTGCCGATGGT
GAGAGTAAGCCCTGTCCCCGACCCACTATCACAAATCAGGGCTGTACCATAGATGAGGAGCCTGGGAACC
CGCTCAGGTTTCTTCTGGTACCAGGCTTAGTAGCTGCTAACACTGACTGGCCCTGCAAGTCAGGGTGGCT
TTTTTCTCCAGAGACAAAGACAGGGAAGCTGGAGACTGTGTCATCACTGTTTC
> (+) T1 NC_000010.11:42185339-42185791 Homo sapiens chromosome 10, GRCh38.p7 Primary Assembly, ENSG00000237592(PSEUDO)
CTCCTGGGGCTCCTGGTGCTCTGGCTGCCAGGTAAGGAAGGAGAACACTAGGATTATACTCGGTCAGTGT
GCTCAGTACTGTCTGGAACTTCAGGGAAGTCCTCTGATAACATGATTAATTGCAAGAATATTTGTTTTTA
TGTTTCCAACTTCAGGTGCCAGATGTGACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGT
AGGAGACAGAGTCACCATCACTTGCCGGGCGAGTCAGGGCATTAGCAATAATTTAAATTGGTATCAGCAG
AAACCAGGGAAAACTCCTAAGCTCCTGATCTATGCTGCATCCAGTCTGCAAAGTGGGATTCCCTCTCGGT
TCAGTGACAGTGGATCTGGGACAGATTACACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAAC
TTATTACTGTCAACAGAGTGACAGTACCTCTCC
> (+) T1 NT_187579.1:83359-83641 Homo sapiens chromosome 10 genomic scaffold, GRCh38.p7 alternate locus group ALT_REF_LOCI_1 HSCHR10_1_CTG3, IGKV1OR10-1, ENSG00000237592
GACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCC
GGGCGAGTCAGGGCATTAGCAATAATTTAAATTGGTATCAGCAGAAACCAGGGAAAACTCCTAAGCTCCT
GATCTATGCTGCATCCAGTCTGCAAAGTGGGATTCCCTCTCGGTTCAGTGACAGTGGATCTGGGACAGAT
TACACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTACTGTCAACAGAGTGACAGTA
CCT
> (-) T1 NC_000009.12:40641828-40642110 Homo sapiens chromosome 9, GRCh38.p7 Primary Assembly, IGKV1OR9-2(PSEUDO), ENSG00000225380
GGTTACTGTCACTCTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGT
GTAATCTGTCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGATGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCTTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGCCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (-) NC_000009.12:63441047-63441329 Homo sapiens chromosome 9, GRCh38.p7 Primary Assembly, LOC107987009
GGTTACTGTCACTCTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGT
GTAATCTGTCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGATGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCTTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGCCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (-) T1 NC_000009.12:64765058-64765340 Homo sapiens chromosome 9, GRCh38.p7 Primary Assembly, IGKV1OR-2(PSEUDO), ENSG00000156755
GGTTACTGTCACTCTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGT
GTAATCTGTCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGATGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCTTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGCCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (+) T1 NC_000009.12:65771148-65771430 Homo sapiens chromosome 9, GRCh38.p7 Primary Assembly, ENSG00000204776(PSEUDO)
GACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGGCAGAGTCACCATCACTTGCC
GGGCGAGTCAGGGCATTAGCAATAATTTAAATTGGTATCAGCAGAAACCAAGGAAAACTCCTAAGCTCCT
GATCTATGCTGCATCCAGTCTGCAAAGTGGGATTCCCTCTCGGTTCAGTGACAGTGGATCTGGGACAGAT
TACACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAACCTATTACTGTCAACAGAGTGACAGTA
ACC
> (-) T1 NC_000009.12:65250543-65250826 Homo sapiens chromosome 9, GRCh38.p7 Primary Assembly, IGKV1OR9-1, ENSG00000204780
TCTGTTGACAGTAATAGGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGTGTAATCTGTCCC
AGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGATGCAGCATAGATCAGGAGCTTA
GGAGTTTTCCTTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCACCCGGCAAGTGA
TGGTGACTCTGCCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGATGTCACATCTGAC
ACCT
> (-) T1 NC_000022.11:10685691-10685973 Homo sapiens chromosome 22, GRCh38.p7 Primary Assembly, IGKV1OR10-1, ENSG00000237592
GGATACTGTCACTCTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGT
GTAATCTGTCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGATGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCCTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (-) T1 NC_000022.11:16904219-16904696 Homo sapiens chromosome 22, GRCh38.p7 Primary Assembly, ENSG00000230481 (PSEUDO) IGKV1OR22-5
GGAGGGGTACTGTAACTCTGTTGACAGTAATAAGTTGTAAAATCTTCAGGCTGCAGGCTGCTGATGGTGA
GAGTCTAATCTGTCCCAGATCCACTGTCACTGAACTGAGAGGGAATCCCACTTTGCAGACTGGATGCAGC
ATAGATCAGGAGCTTAGGAGTTTTCCCTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGA
CTCGCCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCT
GGATGTCACATCTGGCACCTGCAGTTGGAAACATAAAAACAAATATTCTTGCAATTAATCATGTTATCAG
AGGACTTCCCTGAGGTTCCAGACAGTACTGAGCACACTGACCGAGTATAATCCTAGTGTTCTCCTTCCTT
ACCTGGCAACCAGAGCACCAGGAGCCCCAGGAGCTGAGTGGGGGACCTTGCATCCGTG
> (-) T1 NC_000022.11:16933520-16933820 Homo sapiens chromosome 22, GRCh38.p7 Primary Assembly, ENSG00000253481 (PSEUDO) IGKV1OR22-1
AGGAGGGTAACTGTAATGCTGTTGATAGTAATAAGTGGCCAAATCATCACGCTGCAGGCTGCAGGCTGCT
GATGGTGAGAGTGAAATCTGTCCCAGATTGACTGCTACTGAACCAGGATGGGACCCCCGTCTGCAGTTTT
GTTGCAGCATGAATTAGGAGAGTAGGGGCTTTCCCTGGTTTCTGCTGATACCAGACTAATTTATTACTAA
TGCTGTGACTCACCTGGCAAGTGATAGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTG
GGTCATCTGGATATCACGTCT
> (-) T1 P NC_000022.11:16914240-16914542 Homo sapiens chromosome 22, GRCh38.p7 Primary Assembly, ENSG00000253691 (PSEUDO) IGKV2OR22-4
AGTTTGTAGAGCTTGCATGCAGTAATAAACCCCAACATCCTAAGCCTCCACCCTACTGATTTTCAGAGTG
AAATCAGTGCCTGACCCACTGCCACTGAACCTGTCTGGAACTCCAGAGGCCCGGTTGGAAACCTCATAGA
TCAGGAGCTGTGGAGACTGGCCTGGCTTCTGCAGGTACCAATTCAAATAGGTGTATTCATCATCAGTATC
CAAGAGGCTCTCACTAGATCTGCAGGAGATGGAGGCTGGCTCTCCAGGAGTGACAGGCAGGGAGAGTGGA
GTCTGGGTCATCACAATGTCCCC
> (-) T1 P NC_000022.11:16925916-16926200 Homo sapiens chromosome 22, GRCh38.p7 Primary Assembly, ENSG00000254264 (PSEUDO) IGKV3OR22-2
AACAAACAAAGATTAAAAAAAAAGACAAAGAAGTGAAAAATCTTAGGCTTCAGGCAGCTGATGGTGATAG
TAAAGTCTGTCTCCAATCCATGACCACTAAACCCCAGGATGCTAGTGGCCCTGTTGGATGTGCCTTAGAT
GAGGAACCAGGGAGCTTTTCCAGGTTTCTGCTGATACCAGGCTAAGGAGCTGCCAATGCTCTGACTGCAC
ACACAGATGAGAGAGTCTCTTTTCCCTGAAGACAAAGACAAGGAGTCAAGAGACTGCATCAACATAACTT
CTCTG
> (-) T1 NC_000022.11:16921440-16921730 Homo sapiens chromosome 22, GRCh38.p7 Primary Assembly, ENSG00000253460 (PSEUDO) IGKV2OR22-3
GTGGGAGGAGTTTGTAGAGCTTGCATGCAGTGATAAACCCCAACATCTTCAGCCTCCACCCGGCTGATTT
TCAGTGTGAAATCAGTGCCTGACCCACTGCCACTGAGCCTGTCTGGGACTGCAGAGGCCCGGTTCAAAAC
CAAATAGATCAGGAGCTGTAGAGACTGGCCTGGCTTCTGCAGGTACCAAATAGGTTTATTCCCCCCTGTA
TACAAGGCTGTGACTAGACCTGCAGAAGGAGATGGAGGCCAGCTATCCAGGGGTGACGAGCAGGGAGAGT
GGAGTTTGGGT
> (+) T1 NT_187524.1:86871-87153 Homo sapiens chromosome 2 genomic scaffold, GRCh38.p7 alternate locus group ALT_REF_LOCI_1 HSCHR2_1_CTG7, IGKV1OR2-118(PSEUDO)
GACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCC
GGGCGAGTCAGGGCATTAGCAATAATTTAAATTGGTATCAGCAGAAACCAGGGAAAACTCCTAAGCTCCT
GATCTATGCTGCATCCAGTCTGCAAAGTGGGATTCCCTCTCGGTTCAGTGACAGTGGATCTGGGGCAGAT
TACACTCTCACCATCCGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTACTGTCAACAGAGTGACAGTA
CCC
> (+) P NT_187367.1:39216-39498 Homo sapiens chromosome 1 unlocalized genomic scaffold, GRCh38.p7 Primary Assembly HSCHR1_CTG7_UNLOCALIZED, NONE
GACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCC
GGGCGAGTCAGGGCATTAGCAATAATTTAAATTGGTATCAGCAGAAACCAGGGAAAACTCCTAAGCTCCT
GATCTATGCTGCATCCAGTCTGCAAAGTGGGATTCCCTCTCGGTTCAGTGACAGTGGATCTGGGGCAGAC
TACACTCTCACCATCCGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTACTGTCAACAGAGTGACAGTA
CCC
> (+) T1 NC_000001.11:144085812-144086094 Homo sapiens chromosome 1, GRCh38.p7 Primary Assembly, ENSG00000276674 (PSEUDO) IGKV1OR1-1
GACATCCAGATGACCCAGTCTCCATCCTCCCTGTCTGCATCTGTAGGAGACAGAGTCACCATCACTTGCC
GGGCGAGTCAGGGCATTAGCAATAATTTAAATTGGTATCAGCAGAAACCAGGGAAAACTCCTAAGCTCCT
GATCTATGCTGCATCCAGTCTGCAAAGTGGGATTCCCTCTCGGTTCAGTGACAGTGGATCTGGGGCAGAC
TACACTCTCACCATCCGCAGCCTGCAGCCTGAAGATTTTGCAACTTATTACTGTCAACAGAGTGACAGTA
CCC
> (-) T1 NC_000001.11:144874614-144874896 Homo sapiens chromosome 1, GRCh38.p7 Primary Assembly, LOC107985528, ENSG00000224363
GGGTACTGTCACTCTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCGGATGGTGAGAGT
GTAGTCTGCCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGATGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCCTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (-) T1 NT_187648.1:128240-128522 Homo sapiens chromosome 2 genomic scaffold, GRCh38.p7 alternate locus group ALT_REF_LOCI_2 HSCHR2_2_CTG7, IGKV1OR2-118 (PSEUDO)
GGGTACTGTCACTCTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCGGATGGTGAGAGT
GTAATCTGCCCCAGATCCACTGTCACTGAACCGAGAGGGAATCCCACTTTGCAGACTGGGTGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCCTGGTTTCTGCTGATACCAATTTAAATTATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (+) NT_187648.1:2760-3050 Homo sapiens chromosome 2 genomic scaffold, GRCh38.p7 alternate locus group ALT_REF_LOCI_2 HSCHR2_2_CTG7, NONE
GTGTCATCTGGATGACCCAGTCTCCATCCTTACTCTCTGCATCTACAGGAGACAGAGTCACCATCAGTTG
TCGGATGAGTCAGGGCATTAGCAGTTATTTAGCCTGGTATCAGCAAAAACCAGGGAAAGCCCCTGAGCTC
CTGATCTATGCTGCATCCACTTTGCAAAGTGGGGTCCCATCAAGGTTCAGTGGCAGTGGATCTGGGACAG
ATTTCACTCTCACCATCAGTTGCCTGCAGTCTGAAGATTTTGCAACTTATTACTGTCAACAGTATTATAG
TTTCCCTCCCA
> (+) T1 NT_187648.1:41442-41726 Homo sapiens chromosome 2 genomic scaffold, GRCh38.p7 alternate locus group ALT_REF_LOCI_2 HSCHR2_2_CTG7, IGKV3D-7 ENSG00000228325
GAAATTGTAATGACACAGTCTCCAGCCACCCTGTCTTTGTCTCCAGGGGAAAGAGCCACCCTCTCCTGCA
GGGCCAGTCAGAGTGTTAGCAGCAGCTACTTATCCTGGTACCAGCAGAAACCTGGGCAGGCTCCCAGGCT
CCTCATCTATGGTGCATCCACCAGGGCCACTGGCATCCCAGCCAGGTTCAGTGGCAGTGGGTCTGGGACA
GACTTCACTCTCACCATCAGCAGCCTGCAGCCTGAAGATTTTGCAGTTTATTACTGTCAGCAGGATTATA
ACTTA
> (-) T1 NC_000024.10:11473766-11474048 Homo sapiens chromosome Y, GRCh38.p7 Primary Assembly, ENSG00000271375 (PSEUDO)
GGGTACTGTCACTCTGTTGACAGTAGTAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGGGAGT
GTAATCTGTCCCAGATCCACTGTCACTGAACCGAGTGGGAATCCCACTTTGCAGACTGGATGCAGCATAG
ATCAGGAGCTTAGGAGTTTTCCCTGGTTTCTTCTGATACCAATTTAAATTATTGATAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (-) T1 NW_012132915.1:428453-428735 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-39
GGGTACTGTAACTCTGTTGACAGTAGTAAGTTGCAAAATCTTCAGGTTGCAGACTGCTGATGGTGAGAGT
GAAATCTGTCCCAGATCCACTGCCACTGAACCTTGATGGGACCCCACTTTGCAAACTGGATGCAGCATAG
ATCAGGAGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAATTTAAATAGCTGCTAATGCTCTGACTTG
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (-) T1 NW_012132915.1:322251-322533 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-27
GGGCACTGTTATACTTTTGACAGTAATAAGTTGCAACATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGT
GAAATCTGTCCCAGATCCACTGCCACTGAACCGAGATGGGACCCCTGATTGCAAAGTGGATGCAGCATAG
ATCAGGAGCTTAGGAACTTTCCCTGGTTTCTGCTGATACCAGGCTAAATAATTGCTAATGCCCTGACTCG
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGAT
GTC
> (-) T1 NW_012132915.1:208695-209000 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-16
TTATACTGTTGGCAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGTGAAATCTG
TCCCAGATCCACTGCCGCTGAACTTTGATGGGACCCCACTTTGCAAACTGGATGCAGCATAGATCAGGGA
CTTAGGGGCTTTCCCTGGTTTCTGCTGAAACCAGGCTAAATAATTGCTAATGCCCTGACTCGCCCGACAA
GTGATGGTGACTCTGTCTCCTACAGATGCAGACAGTGAGGATGGAGACTGGGTCATCTGGATGTCACATC
TGGCACCTGAGATTGGAAACATAAAA
> (-) T1 NW_012132915.1:226165-226455 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-17
GGGAGGGTAACTATTATGCTGTAGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATTGTG
AGAGTGAATTCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTGCAAACTGGATGCAG
CATAGATCAGGCGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAGCCTAAATCATTTCTAATGCCCTG
ACTTGCCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATC
TGGATGTCACA
> (-) T1 NW_012132915.1:75100-75385 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-6
ATCTTGTAGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGTGAAATCTGTG
CCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTGTAAACTGGATGCAGCATAGATCAGGAGCT
TAGGGGCTTTCCCTGGTTTCTGCTGATACCAGCCTAAATCATTTCTAATGCCCTGACTTGCCCGGCAAGT
GATGGTGACTCTGTCTCCAACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGATGGCACATCTG
GCACCT
> (-) T1 NW_012132915.1:406090-406375 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-37
AGGGGCATTGTAAGTCCGTTGACCGTAATAAGTTGCAACATCTTCAGGCTGCAGGCTGCTGATAGTGAGA
GTGAAATCTGTCCCAGATCCACTGCCACTGAACCGAGATGGGACTCCAGATTGCAAATTGGATGCACTAT
AGATCAGGAGCTTAGGAACTTTCCCTGGTTTCTGCCGATACCAATTTAAATAACTGCTAATGCCCTGACT
CACCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCAACTGG
ATGTCA
> (-) T1 NW_012132915.1:154810-155100 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-13
TATGTGAGGGTAATTATTAAACTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATG
GTGAGAGTGAAATCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTCCAAACTGGAGG
CATCATAGATCAGGAGCTTAGGAGCTTTCCCTGGTTTCTGCTGATATCAGGCTAAAGCACTGCTAATGCC
CTGACTTGCCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTC
AACTGGATGGC
> (-) T1 NW_012132915.1:118810-119092 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-9
GGTAACTATTAAGCTGTTGACAGTAATAAGTTGCAAAATCTTCAGGCTGCAGGCTGCTGATTGTGAGAGT
GAATTCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTGCAAAGTGGATGCAGCATAG
ATCAGGAGCTTAGGGGCTTTCCCTGGTTTTTGCTGATACCAGGCTAAATAACTGCTAATGCCCTGACTGG
CCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGAAGGATGGAGACTGGGTCAACTGGAT
GTC
> (-) T1 NW_012132915.1:149040-149334 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-12
ACACTGTGGGAGGGAAACTGTTAGCCTGTTGACAATAGTAAGTTGCAAAATCTTCAGGCTGCAGGCTGCT
GATGGTGAGAGTGAAATCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTGCAAACTG
GATGCAGCATAGATCAGGAGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAGGCTAACCAGCTGCTAA
TACCCTGACTCGCCCGACAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACACGGAAGATGGAGACTG
GGTCATCTGGATGTC
> (-) T1 NW_012132915.1:376830-377115 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-33
GAGATTATCATACTGTTGACAGTAATATGTTGCAATATCTTCAGGCTGCAGGCTGCTGATGGTGAAAGTA
AAATCTGTCCCAGATCCACTTCCACTGAACCTTGATGGGACCCCTGTTTCCAAATTGGATGCATCGTAGA
TCAGGAGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAATTTAAATAGTTGCTAATGTCCTGACTCGC
CTGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGAGGATGGAGACTGGGTCATCTGGATG
TCACAT
> (-) T1 NW_012132915.1:101230-101520 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-8
GTGGGAGGGTAACTATAATACTGTTGACAGTAATAAGTTGCAAAATCTTCAGACTGCAGGCAGCTGATGG
TGAGAGTGAAATCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTGCAAAGTGGATGC
AGCATAGATCAGGAGCTTAGGGGCTTTCCCTGGTTTTTGCTGATACCAGGCTAAATAACTGCTAATACCC
TGACTCGCCCGACAAGTGATGGTGACTCTGTCTCCTGTAGATGCAGAGAATGAGGATGGAGACTGGGTCA
TCCGGATGGCA
> (-) T1 NW_012132915.1:395528-395818 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-35(PSEUDO)
ATTTTTATACTGTTGACAGTAATAAGTTGCAACATCTTTAGGCTGCAGGATTCTGATGGTGAGAGTAAAA
TCTGTCCCAGATCCACTGCCACCGAACCGCGAAGGAGCCCCAGATTGCAAACTGGATGCAGCATAGATCA
GGCCCTTAGGGGCCTTCCCTGGTTTCTGCTGATACCAGTCTAAATTACTACCAATGCTCTGACTCGCCCG
GCAAGTGATGGTGACACTGTCTCCTTACAGATGCAGACAGTGTGGATGGAGACTGGGTGACTGGATGTCA
CTTCTGGTCCC
> (-) T1 NW_012132915.1:56128-56411 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-5
GAATAACTATTATACTGTTGGCAGTAATAAGTTGCAAAATCATCAGGCTGCAGGCTGCTGATGGTGAGAG
TGAATTCTGTCCCAGATCCACTGCCGCTGAACCTTGATGGGACCCCACTTTCTAAACTAGACGCCTTATA
GATCAGGAGCTTAGGGGCTTTCCCTGGTTTCTGCTGATACCAGGCCAACCAGCTACTAATACTCTGACTG
GCCCGGCAAGTGATGGTGACTCTGTCTCCTACAGATGCAGACAGGGTGGAAGGAGACTGGGTCATCTGGA
TGTC
> (-) T1 NW_012132915.1:279570-279860 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-22 (PSEUDO)
GATGGCTGCTGTAAGTCTATAGACAGCAATAAGTTATAACATCTTCAGGTTGCAGGCTCCTGATGGTGAG
AATGTGTGAAATGTGTCCCAGACCTACTGCCACTGAACCGTGACGGGACCCCAGATTGCAAACTGGATGC
AGCATAGATCAGGAGCTTAGGAGGATTCTCTAGTTTCTACTGATACTAGCTTAAATAATTGCAAATGCCC
TGACTCGCCCAGCAAGTGATGGTGACTCTCTCTCCTACAGATGCAGTCAGGGAGGATGGAGACTGAGTCA
TCTGGAAATTA
> (-) T1 NW_012132915.1:194005-194287 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV3-15
GCCAGTTATTATACTGCTGACAGTAATAAACTGCAAAATCTTCAGACTGCAGGCTGCTGATGGTGAGAGT
GAACTCTGTCCCAGACCCACTGCCACTGAACCTGGCTGGGATACCAGTGGCCCTGGTGGATGCACCATAG
ATGAGGAGCCTGGGAGCCTGGCCAGGTTTCTGCTGGTACCAGGCTAAGTTGCTGCTAACACTCTGACTGG
CCCTGCAGGAGAGGGTGGCTCTTTCCCCTGGAGACACAGACAGGGTGGCTGGAGACTGCGTCATCACTAT
TTC
> (-) T1 NW_012132915.1:87297-87581 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV3-7
TAAGTTATAATCCTGCTGACAGTAATAAACTGCAAAATCTTCAGGCTGCAGGCTGCTGATGGTGAGAGTG
AAGTCTGTCCCAGACCCACTGCCACTGAACCTGGCTGGGATGCTAGTGGCCCTGGTGGATGCACCATAGA
TGAGGAGCCTGGGCGCCTGGCCAGGTTTCTGCTGATACCAGGTTAAGTAGCTGCTGCTAACACTCTGACT
GGCCCTGCAGGAGAGGGTGACTCTTTCCCCTGGAGACAAAGACAGGGTGGGTGGAGACTGTGTCATTACA
ATTTC
> (-) T1 NW_012132915.1:362374-362657 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV1-32 (PSEUDO)
CTTTTATACTGTTGACCAATAATAAGAAGTTGCAGCAACTTCAGACTGGAGGATGCTAATGGTGAGAATC
AAATCTGTCCTGGATCCAATGCCACATAACTGCAATGGGACCCAGGTTTGCAAATTGGATGCATCGTAGA
TCAGGAGCTCAGAAGCTTTCCCTGGCTTCTCTTTGTATCAGGCTAAAACATGGCTAATGCCCTGCCTGAC
TTTCCTGGCATGTGATGGTGACTCTCACCTAGACAGGAAGACAGCGAGGATGGAGACTGGGTCATCTGCA
TGTC
> (-) T1 NW_012132915.1:135990-136281 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV3-11
CTGTGGGAGGCCAGTTGCTACGCTGCTGACAGTAATAAACTGCAAAATCTTCAGGCTCTAGGCTGCTGAT
GGTGAGAGTGAAGTCTGTCCCAGACCCACTGCCACTGAACCTGGCTGGGATGCCAGTGGCCCTGTTGGAT
GCATCATAGATGAGGAGCCTGGGAGCCTGGCCAGGTTTCTGTTGGTACCAGGCTAAGTAGCTGCTAACAC
TCTGACTGGCCCTGCAGGAGAGGGTGGCTCTTTCCCCTGGAGACAAAGACAGGGTGGCTGGAGACTGTGT
CAACACAATTTC
> (-) T1 NW_012132915.1:268575-268861 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV6-21
TGAGGTAAACTACTACTCTGATGACAGTAATACGTTGCAGCATCTTCAGCTTCCAGGCTATTGATGGTGA
GGGTGAAATCTGTCCCAGATCCACTGCCACTGAACCTCGAGGGGACCCCTGAGAAGGACTGGGAAGCATA
CTTGATGAGGAGCTTTGGAGACTGATCTGGTTTCTGCTGGTACCAGTGTAAGCTACTACCAATGCTCTGA
CTGGCCCGGCAGGTGATGGTGACTTTCTCCTTTGGAGTCACAGACTGAAAGTCTGGAGACTGAGTCAGCA
CAATTTC
> (-) T1 NW_012132915.1:251400-251934 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV3-20
AGGTGAGCTACCATACTGCTGACAGTAATACACTGCAAAATCTTCAGGCTCCAGTCTGCTGATGGTGAGA
GTGAAGTCTGTCCCAGACCCACTGCCACTGAACCTGTCTGGGATGCCAGTGGCCCTGCTGGATGCACCAT
AGATGAGGAGCCTGGGAGCCTGGCCAGGTTTCTGCTGGTACCAGGCTAAGTAGCTGCTGCTAACACTCTG
ACTGGCCCTGCAGGAGAGGGTGGCTCTTTCCCCTGGAGACAAAGACAGGGTGCCTGGAGACTGCGTCAAC
ACAATTTCTCCGGTGGTATCTGAGATTGGAAATAAAACAGAAAAGTCACCCATGTAATCTAAATCAAACC
CATTGTCTTCCCAGAAGAGCCAGAATTATTGCTTTATATTGAGCTTTAATTATTGTATTGACTGAGCAGA
GTTGCCAGGTAACAGGACTTGAGAGGGTTTTCACTGACATGCAAAACCATCCCATGTTCCCCTCACCTGG
GAGCCAGAGTAGCAGGAGGAAGAGAAGCTGCGCTGGGGTTTCCAT
> (-) T1 NW_012132915.1:23906-24504 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH,IGKV7-3(PSEUDO)
AGGAAAATTCTTACTCTGCAGACAGTAATAATTTGCAGTATCATTAGCTTCCACAGGATTAATTGTGAGG
GTGAAATCGGTCCCAGACCCACTGCCGCTGAACCTGGCTGGGACCCCAGTGTCTTTATTGGATGCTTGGT
AAATCAGGAGTTTAGGAGGTTGTCCTGGTTTCTGCTGATACCAGTGAATTAAGTTTATTCCCAAGAAACT
GACACTCTCACTGGCTCTGCAGGTGATGGTGGCCCTCTGTCCTGGAGACACGGCCAAGGAGGCTGGAGAC
TGGGTCAGCACAATGTCCCCATTGCAGCCTGAAATGATAAAGACAGATAAATTATATCAGATATACTGAG
ACTGTCCCCATGTAGGCCATGCATTGGTGACACTTGTAACCACAGTCATATGCAACATCTTGAGTAACCA
GAAAACAAAAGATAACTGGGGAACTTACAACCTACAATGAGTGCCCTAAATCCAACAACCAAGAATCCAG
AGACACAAAAAACAATGATGGCCACATGAGTTTGCCCGATGTTTCCCTATACCCCCTCACTTGGAGCCCA
GAGCAGGAGGATCCACAGCAAAGGAGCCCCGGACCCTAT
> (-) T1 P NW_012132915.1:330524-330825 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV2-28
AGGAGTTTGTAGAGCTTGCATGCAGTAATAAACCCCAACATCCTCAGCCTCCACTCTGCTGATTTTCAGT
GTAAAATCTGTGCCTGATCCACTGCCACTGAACCTGTCAGGGACCCCGGAGGCCCGATTAGAACCCAAAT
AGATCAGGAGCTGTGGAGACTGCCCTGGCTTCTGCAGGTACCAATCCAAATAGTTGTATCCATTACTATG
CAGGAGGCTCTGACTAGACCTGCAGGAGATGGAGGCCGGCTCTCCAGGGGTGACGGGCAGGGAGAGTGGA
GACTGAGTCATCACAATATCCC
> (-) T1 P NW_012132915.1:304900-305204 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV2-26(PSEUDO)
TGGGAGGATCTTGTGCATCTTGCATGCAGTAATAAACTCCAACATCCTCAGCCTCCACCCGGCTGATTTT
CAGTGTGAAATCTGTCCCTGACCCGCTGCCACTGAACCTATCTGGCACTCCAGAGAACCGGTTGGAAACT
TCATAGATCAGGAGCTGTGGAGACTGGCCTGGCTTTCTGCAGAAACCAATACAAATAGGTGTATCCATCA
CTATGCAGGAGGCTCTGACTAGACCTGCAGGACATGGAGGCCTGCTCTCCAGGGGTGATAGACAAGGAGA
GTGGAGTCTGGGTCATCACAATCTC
> (-) T1 P NW_012132915.1:343010-343310 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV2-29(PSEUDO)
GAGGAAGGTGTATACCTTGCATTCAGTAATAAACCCCAACATCCTCAGCCTCCACCCGGCTGATTTTCAG
TGTGAAATCTGTCCCTGACCCGCTGCCACTGAACCTATCTGGCACTCCAGAGAACCGGCTGGAAACTTCA
TAGATCAGGAGCTGTGGAGACTGGCCTGGCTTCTGCAGGTACCAATACAAATAGGTCTTTCCATCACTAT
GCAGGAGGCTCTGACTAGACTTGCAGGAGATGGAGGCCGGCTGTCCAGGGGTGACGGACAGAGAGAGTGG
AGTCTGGGTCATCACAATATC
> (-) T1 P NW_012132915.1:438944-439244 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV2-40
GAAACTCTATACGTTGCATGCAGTAATAAACTCCAACATCCTCAGCCTCCACCCTGCTGATTTTCAGTGT
GAAATCAGTGCCTGACCCACTGCCACTGAACCTGTCTGGGACTCCAGAGGCCCGATAGGAAAGCGTATAG
ATCAGGAGCTGTGGAGACTGCCCTGGCTTCTGCAGGTACCAGTCCAAATAGGTGTTTCCATCATCACTAT
CCAAGAGGCTCTGACTAGACCTGCAGGAGATGGAGGCCGGCTCTCCAGGGGTGACGGGCAGGGAGAGTGG
AGTCTGGGTCATCACAATATC
> (-) T1 NW_012132915.1:361020-361306 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV3-31(PSEUDO)
TGGAATACCCACCACTATGCTGATAACAGTGTTAAAGTGCAAAATCTTCATGCTCCAGCCTGCTGATAAT
GAGACTGAAGTTTTCCCCGAACCCACTGCCACTCCACCAGGCTGGGACATTGGTGGTCCTGGTGGATGCA
CCATGGATGAGGAGCCTGAGAGCCTGTCCAGGTTTCCACTGATACCCTGCTAAGGAGCTGCTAATAGTCT
ACTTGGCTCTGTAGGTGAGGGTGGCTTTTTCCCCTAGAGATAAAGACAGGGAGGCTGGAGACTGTCATCA
CAAGTTC
> (-) T1 NW_012132915.1:237532-238308 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV2-18(PSEUDO)
AGGAAACTGTGTAGCTTGCATGCAGTAATAAACCCCAACATCCTCAGCCTCCACCCAGCTGATTTTCAGT
GTGAAATCACTACCTGACCCACTGCCACTAAACCTGTCTGGGACCCCAGAAAGATGATTGGAAACCCTAT
AAATCAGGAGCTGTGGAGACTGCCCTGGCTTCTGCAGGTACCAATGCAAATAGGTATATCCATTACTATG
CAGGAGGCTCTGACTAGACCTGCAAGAGATGGAGGCCGGCTCTCCAGGGTTGACGGGCAGGGAGGGTGGA
GTCTGGGTCATCACAATATCTCCACTGGATCCTGAAATAGTGAGAGAAGTGCAAAGTTATGTACAAATAT
TGGGAACCATTGAAATGATATTCTTTCTGTTATCTACTTTATGCTAAGTGATTTTTTTGTGTGACTTTGG
TTCATACCCCTAAACATCCAGGCATAAAAAGAACCAACATTCACAAGGCACAAAAGAGACTCAAGAAGTC
GCCTACACTATTATCCTCTTCCTGTGTGACACTCTTCATGAGAGCACAAGTCCTTTGTCCTTCTAGGATA
TGAAGTTTAGAACTATAAGAGTGAGGAATCTTCTCTTTCTGACTCTTGCAGTTCTAAACTTTATACACCT
TTTCTTGCAGGTCAAGATGTGCATGTGGACAGGCAGTGGGACCCCCAGAGCTCACCCTCACACTCCATTC
TCCTCCCTTATCTCCCTTCTGTCCTTACCAGGAACCCAAAGCATTAGCAGCCCCAGGAGCTGAGCAGGGA
CCCTTAT
> (+) T1 NW_012132915.1:6315-6607 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV5-2
ATACCAGGGCAGAAACGACACTCACGCAGTCTCCAGCATTCATGTCAGCGACTCCAGGAGACAAAGTCAA
CATCTCCTGCAAAGCCAGCCAAGACATTGATGATGATATGAACTGGTACCAACAGAAACCAGGAGAAGCT
GCTATTTTCATTATTCAAGAAGCTACTACTCTCGTTCCTGGAATCCCACCTCGATTCAGTGGCAGCGGGT
ATGGAACAGATTTTACCCTCACAATTAATAACATAGAATCTGAGGATGCTGCATATTACTTCTGTCTACA
ACATGATAATTTC
> (-) T1 P NW_012132915.1:353600-353906 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV2-30
CTGTGGGAGGCCAGTGTGTACCTTGCATGCAGTAATAAACCCCAACATCCTCAGCCTCCACCCTGCTGAT
TTTCAGTGTGAAATCAGTGCCTGACCCACTGCCGCTGAATCTGTCTGGGACCCCAGAGTCCCGGTTAGAA
ACCTTATAAATTAGGCGCCTTGGAGATTGGCCTGGCCTCTGCTGAAACCAATTCAAGTAGGTGTTTCCAT
CACTGTATACGAGGCTTTGACTAGACCTGCAGGAGATGGAGGCCGGCTGTCCAAGGGTGACGGGCAGGGA
GAGTGGAGACTGAGTCATCACAACATC
> (-) T1 P NW_012132915.1:301295-301600 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV3-25(PSEUDO)
TGTTGCATGTCGAATCAGTATGGGACACCAACTACTATGCTGATAACAGTGATGAAGTGCAAATCTCCAG
GCTCCAGGCTCCAGGCTGCCGATGGTGAGAGTAAGCCCTGTCCCCGACCCACTATCACAAATCAGGGCTG
TACCATAGATGAGGAGCCTGGGAACCCGCTCAGGTTTCTTCTGGTACCAGGCTTAGTAGCTGCTAACACT
GACTGGCCCTGCAAGTCAGGGTGGCTTTTTTCTCCAGAGACAAAGACAGGGAAGCTGGAGACTGTGTCAT
CACTGTTTCTACAGTGAAATCTGAGA
> (-) T1 P NW_012132915.1:285154-285460 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV2-24
AGGAAATTGTGTAGCTTGCATGCAGTAATAAACCCCGACATCCTCAGCTTCCACCCTGCTGATTTTCAGT
GTGAAATCTGTCCCTGCCCCACTGCCACTGAATCTGTCTGGGACCCCAGAGAACCGGTTAGAAATCTTAT
AAATTAGGAGTCTTGGAGGCTGGCCTGGCCTCTGCTGAAGCCAACTCAAGTAGGTGTTTCCATCACTGTG
TACGAGGCTTTGACTAGACCTGCAGGAGATGGAGGCCGGCTGTCCAAGGGTGACAGGTGAGGAGAGTGGA
GTCTGGGTCATCACAATATCCCCACTG
> (-) T1 P NW_012132915.1:317060-317365 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGK
ACAGGCAAGCTCCTATGTTGTTGACAGTAACAGTACGCTGCATCTTCAGCCTCCAGGCTGCTGATGGAGG
GGATGAAATCAGTCCACCCACTGTCACTAATCCTGGCAAGGACAGCAAGGTGCAGGTCATAATTACTATA
AATAGTAAGATTCAGAGCCTGACCTGGTTTTTGTTGGCTCCAATTCAGGCAGCTACAAATATCGTCACAG
CTTCTCAGCTGATGGTGGCCTTTCAACTTCTCTCAGGAAGCTTTGTCTGGAAGTTTTGTAAGTTTGGGCA
CGATAATGTTCCCGTTGACAACTGAA
> (-) P NW_012132915.1:290300-290600 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGK
GTCACACGAGAGAGGCAAGATTTGATGTTGTTGACAGTAACAGTACCCTGCATCTTCAGGCTTCAGGCTG
CTGATTGTGGGAACAAAATCTACCTCAGACTCGTGGTCACTCAACCATGCAGGGACACTAGGGTTCTGGA
TAGTGGCTTGCTTCCCTCAACCTTAGTCCAGAACTTGAAAATTGAGAACTCATGAACACAAGTAAGGGAA
CAATACACACTGGGGTCTACCTGAGGGTGGAGGGTGGAAGAAAGGAAAGGAGCAGAAAAGATAACTATTG
GGCACTGGGAATAATACCTGG
> (-) T1 P NW_012132915.1:418730-419030 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGKV2-38(PSEUDO)
GGATATTATGTAGCTTGCATGTATTAATAAAGTCGAATATCCTCAGCCTCCACCCTGCTAATTTTGAGTT
TAAAATATGTGCCTGACCCACTGCTATTGAACCTGTCTGGGACTCCAGAGGCCCCATTGGAAACCCCATA
GATCAGGAGCTGTGGAGACTCGCCTGGCTTCTATAGTTACCAATACAAATAGGTGTTTCCATTGCTATGC
AGGAGGGTCTGACTAGACCTGCAGGAGATGAAGTACAAAGTTATGTACAAATATTATGAGCAAGTATCAC
GATTTCCCTTATGATATGGAT
> (+) P NW_012132915.1:102577-102880 Homo sapiens chromosome 2 genomic patch of type FIX, GRCh38.p7 PATCHES HG2290_PATCH, IGK
GACATCATCCTGACCCAGACACCATCCTCCCTGTTAACATCTTTAGGAAAGAGACAATCCCTTATCAAGC
AATTGCCAACTTACATGGAGAAATCAGCTGGATCCAGATGAAACTGGACATGGATTTGCAGTCATTATAT
CTCACATCTCTACTGTGCCAAAAATGTCCCAGCCTGGCTTAGTAGCAGGGGACGTGGATCCAACTACATC
AGCATCAGTGGGCTGCAGCCTAGGACTCCACAAAATTTTACTGATGCCTGACTAGGGGAGACAAATCACA
GTGCTGTAGCCCATGCACAAACCT
> (-) NC_000004.12:79780940-79781238 Homo sapiens chromosome 4, GRCh38.p7 Primary Assembly, NONE
ACAACACACTTCTAAAAACACTGATAACGTAGACTGACTGCAAGAATGCAGAGCAACTAGATTCTTCTTA
TGCTGATGGTGAGAGTGTAAACTGACCTCAACTTGGAGAACTGTTTGGCACTTCCTTAAACATACACTGA
CTGTCCCTGTGACCTAGGATTTCAACTTATAGTATTTACCCAATGGAAAATTTTTAAATGTCTGTATAAA
ACTTGTAAAAGTATTTTCATTGCACTCAGTAATAGTTCAAACTGGAAATAATCCAAATGTATACCAAAAA
GAGGGTGGACAAATTACTG