chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180001214180003TT--18GENIChomozygous61318967
1214180025214180026AC24GENIChomozygous61079796
1214180082214180083CG24GENIChomozygous61079797
1214180539214180540CA34GENIChomozygous61079798
1214180752214180753CT30GENIChomozygous61079799
1214181151214181152T-27GENIChomozygous61079800
1214181330214181331AG23GENIChomozygous61079801
1214181334214181335AG24GENIChomozygous61079802
1214181346214181347GT27GENIChomozygous61079803
1214181349214181350GT27GENIChomozygous61079804
1214181352214181353AT26GENIChomozygous61079805
1214181357214181358AT28GENIChomozygous61079806
1214181360214181361AG25GENIChomozygous61079807
1214181361214181362AG25GENIChomozygous61079808
1214181363214181364AG25GENIChomozygous61079809
1214181391214181392AG27GENIChomozygous61079810
1214181548214181549CT17GENIChomozygous61079811
1214181596214181597C-19GENIChomozygous61079812