chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3131286414131286415GA33GENIChomozygous141544214
3131286892131286893GT49GENICpossibly homozygous136822368
3131288154131288155AG57GENIChomozygous136822370
3131289444131289445AG20GENICheterozygous403078420
3131289444131289445A20GENICheterozygous403078421
3131289458131289459AG27GENIChomozygous136822371
3131289539131289540GA47GENIChomozygous136822372
3131289858131289859AG55GENIChomozygous136822374
3131290010131290011TC47GENIChomozygous136822375
3131293165131293166GA65GENIChomozygous143021035
3131296201131296202GA54GENIChomozygous141544215
3131298240131298241GA46GENIChomozygous141544216
3131298759131298759TTTTCTAGTTCTTACTTCACTACTTC2GENIChomozygous136591032
3131289509131289509ATA40GENIChomozygous136591029
3131298752131298752CA2GENIChomozygous136591030
3131298753131298755GG2GENIChomozygous136591031
3131298761131298761CAAT4GENIChomozygous136591033
3131298765131298766G4GENIChomozygous136591034
3131298771131298771T4GENIChomozygous136591035
3131298775131298780AACCG4GENIChomozygous136591036
3131298783131298783TA5GENIChomozygous136591037
3131298785131298786CG7GENIChomozygous136822380
3131298786131298787CG8GENIChomozygous136822381
3131298789131298790C8GENIChomozygous136591038
3131298791131298795CTCC8GENIChomozygous136591039
3131298796131298798GC9GENIChomozygous136591040
3131298798131298799CA10GENIChomozygous136822382
3131299445131299446CT48GENIChomozygous141544217
3131301167131301176AAAGAACCT55GENIChomozygous141482376
3131301200131301200AG55GENIChomozygous141482377
3131302727131302728GA52GENIChomozygous141544218
3131300596131300597AG54GENIChomozygous136822383
3131301016131301017TC61GENIChomozygous136822384
3131301850131301851GA44GENIChomozygous136822385
3131302792131302793TC43GENIChomozygous141544219
3131303449131303452CAC37GENICpossibly homozygous141482378
3131303556131303558GG13GENICheterozygous147430977
3131308338131308339TC50GENIChomozygous141544220
3131309074131309075TG60GENIChomozygous136822391
3131309830131309830TA37GENIChomozygous136591042