chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180001214180003TT--18GENIChomozygous61318967
1214181330214181331AG24GENIChomozygous61079801
1214181334214181335AG24GENIChomozygous61079802
1214181346214181347GT21GENIChomozygous61079803
1214181349214181350GT21GENIChomozygous61079804
1214181352214181353AT22GENIChomozygous61079805
1214181357214181358AT26GENIChomozygous61079806
1214181360214181361AG26GENIChomozygous61079807
1214181361214181362AG26GENIChomozygous61079808
1214181363214181364AG26GENIChomozygous61079809
1214181752214181753TC7GENIChomozygous61079813