chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1264059544264059545CA22GENIChomozygous960076596
1264060180264060181TA28GENICpossibly homozygous960076597
1264061466264061467TC16GENIChomozygous960076598
1264061991264061992GA10GENIChomozygous960076599
1264062067264062068CA2GENIChomozygous960076600
1264062297264062298TC29GENIChomozygous960076601
1264062381264062382CT22GENIChomozygous960076602
1264062501264062502AG23GENIChomozygous960076603
1264062858264062859GT29GENIChomozygous960076604
1264064003264064004AG28GENIChomozygous960076605
1264064234264064235TG23GENIChomozygous960076606
1264064623264064624GA38GENIChomozygous960076607
1264064641264064642CT38GENIChomozygous960076608
1264064988264064989AG31GENIChomozygous960076609
1264066698264066699TC34GENIChomozygous960076610
1264067060264067061TC16GENIChomozygous960076611
1264067293264067294AG35GENIChomozygous960076612
1264068461264068462TG18GENIChomozygous960076613
1264068572264068573GA26GENIChomozygous960076614
1264069891264069892GA20GENIChomozygous960076615
1264070790264070791CT24GENIChomozygous960076616
1264071209264071210CT21GENIChomozygous960076617
1264071386264071387GA23GENIChomozygous960076618