chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180001214180003TT--12GENIChomozygous61318967
1214180025214180026AC19GENIChomozygous61079796
1214180082214180083CG27GENIChomozygous61079797
1214180539214180540CA31GENIChomozygous61079798
1214180752214180753CT21GENIChomozygous61079799
1214181151214181152T-17GENIChomozygous61079800
1214181330214181331AG16GENIChomozygous61079801
1214181334214181335AG15GENIChomozygous61079802
1214181346214181347GT14GENIChomozygous61079803
1214181349214181350GT15GENIChomozygous61079804
1214181352214181353AT15GENIChomozygous61079805
1214181357214181358AT16GENIChomozygous61079806
1214181360214181361AG16GENIChomozygous61079807
1214181361214181362AG17GENIChomozygous61079808
1214181363214181364AG18GENIChomozygous61079809
1214181391214181392AG17GENIChomozygous61079810
1214181548214181549CT20GENIChomozygous61079811
1214181596214181597C-22GENIChomozygous61079812
1214181752214181753TC13GENIChomozygous61079813