chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85495895954958960AT16GENICpossibly homozygous52640480
85495933054959331CT20GENICpossibly homozygous52640482
85495985554959856CT8GENICheterozygous52640484
85496094854960949A-8GENICheterozygous52977767
85496126354961264GA25GENICpossibly homozygous52640486
85496174554961746GA3GENICheterozygous52640488
85496175654961757T-4GENIChomozygous52640490
85496220154962202GA9GENIChomozygous52640492
85496270554962706AG21GENIChomozygous52640494
85496428554964286TG23GENIChomozygous52640496
85496445454964455AG11GENIChomozygous52640498
85496533654965337CT17GENICpossibly homozygous52640500
85496541554965416CT21GENIChomozygous52640502
85496607154966075CAGA----8GENICpossibly homozygous52640504
85496704454967045CA15GENICpossibly homozygous52640506
85496714254967143GA9GENIChomozygous52640507
85496752854967529CT14GENIChomozygous52640509
85496830454968305CT21GENICpossibly homozygous52640515
85496844754968448CT11GENIChomozygous52640517
85496864154968642CT34GENIChomozygous52640519
85497002254970023GA16GENIChomozygous52640521
85497043354970434GA19GENICpossibly homozygous52640523
85497364354973644GA16GENICpossibly homozygous52640525
85497420454974205CT24GENIChomozygous52640526
85497490654974907GA24GENICpossibly homozygous52640528
85497602754976028GT20GENICpossibly homozygous52640530
85497704754977048TC3GENIChomozygous52640532