chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180001214180003TT--1GENIChomozygous61318967
1214180025214180026AC7GENIChomozygous61079796
1214180082214180083CG20GENIChomozygous61079797
1214180539214180540CA15GENICpossibly homozygous61079798
1214180752214180753CT16GENIChomozygous61079799
1214181151214181152T-15GENIChomozygous61079800
1214181330214181331AG2GENIChomozygous61079801
1214181334214181335AG2GENIChomozygous61079802
1214181346214181347GT2GENIChomozygous61079803
1214181349214181350GT1GENIChomozygous61079804
1214181363214181364AG2GENIChomozygous61079809
1214181391214181392AG12GENIChomozygous61079810
1214181596214181597C-14GENICpossibly homozygous61079812