chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180001214180003TT--9GENICheterozygous61318967
1214180025214180026AC17GENICheterozygous61079796
1214180082214180083CG26GENICheterozygous61079797
1214180539214180540CA21GENICheterozygous61079798
1214180752214180753CT21GENICheterozygous61079799
1214181151214181152T-12GENICheterozygous61079800
1214181330214181331AG7GENIChomozygous61079801
1214181334214181335AG7GENIChomozygous61079802
1214181346214181347GT7GENIChomozygous61079803
1214181349214181350GT6GENIChomozygous61079804
1214181352214181353AT6GENIChomozygous61079805
1214181357214181358AT6GENIChomozygous61079806
1214181360214181361AG6GENIChomozygous61079807
1214181361214181362AG6GENIChomozygous61079808
1214181363214181364AG6GENIChomozygous61079809
1214181391214181392AG14GENICheterozygous61079810
1214181548214181549CT12GENICheterozygous61079811
1214181596214181597C-20GENICheterozygous61079812
1214181752214181753TC22GENICheterozygous61079813