chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85495895954958960AT33GENIChomozygous52640480
85495933054959331CT32GENIChomozygous52640482
85495985554959856CT38GENIChomozygous52640484
85496126354961264GA40GENIChomozygous52640486
85496174554961746GA27GENIChomozygous52640488
85496175654961757T-27GENIChomozygous52640490
85496220154962202GA34GENIChomozygous52640492
85496270554962706AG32GENIChomozygous52640494
85496428554964286TG27GENIChomozygous52640496
85496445454964455AG35GENIChomozygous52640498
85496533654965337CT28GENIChomozygous52640500
85496541554965416CT36GENIChomozygous52640502
85496607154966075CAGA----62GENIChomozygous52640504
85496704454967045CA36GENIChomozygous52640506
85496714254967143GA40GENIChomozygous52640507
85496752854967529CT44GENIChomozygous52640509
85496763754967643AAGTAG------29GENIChomozygous53387661
85496764854967649CCTTTTTTTTTTTTT17GENICpossibly homozygous53508035
85496764854967649CCTTTTTTTTT17GENICheterozygous53431790
85496830454968305CT24GENIChomozygous52640515
85496844754968448CT32GENIChomozygous52640517
85496864154968642CT33GENIChomozygous52640519
85497002254970023GA30GENIChomozygous52640521
85497043354970434GA41GENIChomozygous52640523
85497276154972762AAAGAG9GENIChomozygous53387663
85497364354973644GA21GENIChomozygous52640525
85497420454974205CT40GENIChomozygous52640526
85497490654974907GA30GENIChomozygous52640528
85497602754976028GT40GENIChomozygous52640530
85497704754977048TC11GENIChomozygous52640532