chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180001214180003TT--13GENIChomozygous61318967
1214181330214181331AG10GENIChomozygous61079801
1214181334214181335AG9GENIChomozygous61079802
1214181346214181347GT5GENIChomozygous61079803
1214181349214181350GT5GENIChomozygous61079804
1214181352214181353AT5GENIChomozygous61079805
1214181357214181358AT6GENIChomozygous61079806
1214181360214181361AG6GENIChomozygous61079807
1214181361214181362AG6GENIChomozygous61079808
1214181363214181364AG8GENIChomozygous61079809
1214181752214181753TC14GENIChomozygous61079813