chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180025214180026AC8GENIChomozygous61079796
1214180082214180083CG14GENIChomozygous61079797
1214180539214180540CA26GENICpossibly homozygous61079798
1214180752214180753CT15GENICpossibly homozygous61079799
1214181151214181152T-11GENIChomozygous61079800
1214181330214181331AG5GENIChomozygous61079801
1214181363214181364AG1GENIChomozygous61079809
1214181391214181392AG11GENIChomozygous61079810
1214181548214181549CT2GENICheterozygous61079811
1214181596214181597C-15GENICpossibly homozygous61079812
1214181752214181753TC8GENICpossibly homozygous61079813