chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117937084117937085GC11GENIChomozygous823042687
8117937113117937114GA11GENIChomozygous823042688
8117937599117937600TC10GENIChomozygous823042689
8117938840117938841CA13GENIChomozygous823042690
8117938845117938846G-13GENIChomozygous823042691
8117938987117938989TC--14GENIChomozygous823042692
8117945917117945919GC--11GENIChomozygous823042693
8117948034117948035TC13GENIChomozygous823042694
8117948142117948143TC14GENIChomozygous823042695
8117954073117954074CT10GENIChomozygous823042696
8117956787117956788TTTAGC8GENIChomozygous823042697
8117956795117956796CG13GENIChomozygous823042698
8117960587117960588GA16GENIChomozygous823042699
8117960691117960694GGG---15GENIChomozygous823042700
8117962115117962116AG16GENIChomozygous823042701
8117963462117963463T-11GENIChomozygous823042702
8117963771117963772AG15GENIChomozygous823042703
8117968702117968703TG12GENIChomozygous823042704
8117969150117969151TC13GENIChomozygous823042705
8117969446117969447AG11GENIChomozygous823042706
8117969914117969915TTG11GENIChomozygous823042707
8117972274117972275T-10GENIChomozygous823042708