chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264060117264060118AG57GENIChomozygous773964668
1264060592264060593CA41GENICpossibly homozygous773964669
1264061466264061467TC52GENIChomozygous773964670
1264061991264061992GA25GENIChomozygous773964671
1264062033264062034TG13GENIChomozygous773964672
1264062297264062298TC55GENIChomozygous773964673
1264062381264062382CT46GENIChomozygous773964674
1264062501264062502AG41GENIChomozygous773964675
1264062858264062859GT47GENIChomozygous773964676
1264064003264064004AG51GENIChomozygous773964677
1264064234264064235TG47GENIChomozygous773964678
1264064641264064642CT50GENICpossibly homozygous773964679
1264064988264064989AG58GENIChomozygous773964680
1264065091264065092TC53GENIChomozygous773964681
1264065234264065235GA71GENICheterozygous773964682
1264066698264066699TC39GENIChomozygous773964683
1264067060264067061TC55GENIChomozygous773964684
1264067293264067294AG36GENIChomozygous773964685
1264068063264068064TC57GENIChomozygous773964686
1264068572264068573GA49GENIChomozygous773964687
1264070568264070569CT49GENIChomozygous773964688
1264071386264071387GA37GENIChomozygous773964689