chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180001214180003TT--1GENIChomozygous61318967
1214180025214180026AC21GENIChomozygous61079796
1214180082214180083CG15GENIChomozygous61079797
1214180539214180540CA26GENIChomozygous61079798
1214180752214180753CT33GENIChomozygous61079799
1214181151214181152T-19GENIChomozygous61079800
1214181330214181331AG13GENIChomozygous61079801
1214181334214181335AG13GENIChomozygous61079802
1214181346214181347GT12GENIChomozygous61079803
1214181349214181350GT12GENIChomozygous61079804
1214181352214181353AT9GENIChomozygous61079805
1214181357214181358AT7GENIChomozygous61079806
1214181360214181361AG7GENIChomozygous61079807
1214181361214181362AG7GENIChomozygous61079808
1214181363214181364AG7GENIChomozygous61079809
1214181391214181392AG8GENIChomozygous61079810
1214181548214181549CT15GENIChomozygous61079811
1214181596214181597C-14GENIChomozygous61079812
1214181752214181753TC32GENIChomozygous61079813