chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180001214180003TT--17GENICpossibly homozygous61318967
1214180025214180026AC17GENIChomozygous61079796
1214180082214180083CG19GENIChomozygous61079797
1214180539214180540CA21GENIChomozygous61079798
1214180752214180753CT26GENIChomozygous61079799
1214181151214181152T-18GENIChomozygous61079800
1214181330214181331AG17GENIChomozygous61079801
1214181334214181335AG16GENIChomozygous61079802
1214181346214181347GT16GENIChomozygous61079803
1214181349214181350GT16GENIChomozygous61079804
1214181352214181353AT16GENIChomozygous61079805
1214181357214181358AT17GENIChomozygous61079806
1214181360214181361AG19GENIChomozygous61079807
1214181361214181362AG20GENIChomozygous61079808
1214181363214181364AG21GENIChomozygous61079809
1214181391214181392AG21GENIChomozygous61079810
1214181548214181549CT10GENIChomozygous61079811
1214181596214181597C-19GENIChomozygous61079812