chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115761506115761507CT52GENICpossibly homozygous52826692
8115762016115762029GTCTTTCTCCCCT-------------31GENIChomozygous52826693
8115762581115762582TC57GENIChomozygous52826694
8115762799115762800TTAC32GENICheterozygous52826695
8115762843115762844TC42GENICheterozygous52826696
8115762847115762848TC43GENICheterozygous52826697
8115765572115765573GA59GENICpossibly homozygous52826698
8115766556115766557A-9GENICpossibly homozygous52826699
8115766589115766591AA--16GENICpossibly homozygous52826700
8115766980115766981CT25GENIChomozygous52826701
8115767195115767196AT37GENIChomozygous52826702
8115767357115767358TC60GENIChomozygous52826703
8115767612115767613TC66GENIChomozygous52826704
8115768827115768830TCT---40GENIChomozygous52826705
8115769039115769040TG55GENIChomozygous52826706
8115769090115769091GGCTGGAAGGTC28GENIChomozygous52826707
8115769867115769868TC49GENIChomozygous52826708
8115771862115771863AG39GENIChomozygous52826709
8115772007115772008CCA18GENICpossibly homozygous52826710
8115772285115772286GA53GENIChomozygous52826711
8115772876115772877TC46GENIChomozygous52826712
8115773028115773041TTCTTTTTTTTTT-------------20GENICpossibly homozygous52826713
8115775106115775107CA47GENIChomozygous52826714
8115775284115775285CT57GENIChomozygous52826715
8115775702115775704GT--28GENIChomozygous52826716
8115775713115775723CACACACACA----------14GENIChomozygous52826717
8115775872115775873GA69GENIChomozygous52826718
8115775944115775945GA80GENIChomozygous52826719
8115776245115776246CT53GENIChomozygous52826720
8115776408115776409AG63GENIChomozygous52826721
8115776409115776410TC62GENIChomozygous52826722
8115776604115776605AG42GENIChomozygous52826723
8115777815115777816G-4GENIChomozygous52826724
8115778201115778202TC47GENIChomozygous52826725
8115778236115778237CA51GENICpossibly homozygous52826726
8115778902115778903AG42GENIChomozygous52826727