chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
52414412524144126CA12GENIChomozygous572248578
52414485124144852AG13GENIChomozygous572248579
52414593724145938CT19GENIChomozygous572248580
52414598324145984AG24GENIChomozygous572248581
52414604824146049GC18GENIChomozygous572248582
52414605424146055AG18GENIChomozygous572248583
52414613524146136GC13GENIChomozygous572248584
52414693224146935ACT---39GENIChomozygous714216028
52414694224146943CT40GENIChomozygous572248585
52414720824147209CT25GENIChomozygous572248586
52414722624147227AC20GENIChomozygous572248587
52414727124147272TG25GENIChomozygous572248588
52414736724147368GA16GENIChomozygous572248589
52414751024147511AG32GENICpossibly homozygous572248590
52414755224147553CT30GENICpossibly homozygous572248591
52414757324147574TC32GENICpossibly homozygous572248592
52414772424147725CG25GENIChomozygous572248593
52414793024147931TA14GENICpossibly homozygous572248594
52414799924148008ATATTATGG---------5GENIChomozygous714216029
52414800924148010AC3GENIChomozygous574366180
52414805424148055GA11GENIChomozygous572248595
52414811124148112TC11GENIChomozygous572248596
52414814024148141A-9GENIChomozygous714216030
52414846224148463AG37GENIChomozygous572248597
52414952024149521GA20GENIChomozygous572248598
52414956924149570TC21GENIChomozygous572248599
52414959724149598AG25GENIChomozygous572248600
52414985324149854GA31GENIChomozygous572248601
52415015324150154GA30GENIChomozygous572248602
52415168924151690TTA2GENIChomozygous714216031
52415202324152024T-14GENIChomozygous714216032
52415281824152819TC28GENIChomozygous572248603
52415314824153149TC11GENIChomozygous572248604