chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180001214180003TT--16GENIChomozygous61318967
1214181330214181331AG18GENIChomozygous61079801
1214181334214181335AG19GENIChomozygous61079802
1214181346214181347GT21GENIChomozygous61079803
1214181349214181350GT22GENIChomozygous61079804
1214181352214181353AT23GENIChomozygous61079805
1214181357214181358AT27GENIChomozygous61079806
1214181360214181361AG27GENIChomozygous61079807
1214181361214181362AG27GENIChomozygous61079808
1214181363214181364AG26GENIChomozygous61079809
1214181752214181753TC18GENIChomozygous61079813