chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12970495229704953CT44GENIChomozygous778406684
12970510629705107TA23GENIChomozygous778406685
12970511329705114CT17GENIChomozygous778406686
12970522029705221GA37GENIChomozygous778406687
12970523529705236TC42GENIChomozygous778406688
12970562629705627GA57GENIChomozygous778406689
12970569829705699CT47GENICpossibly homozygous778406690
12970576929705770AC45GENICpossibly homozygous778406691
12970577829705779TG45GENIChomozygous778406692