chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214180001214180003TT--19GENICpossibly homozygous61318967
1214181330214181331AG27GENIChomozygous61079801
1214181334214181335AG28GENIChomozygous61079802
1214181346214181347GT27GENIChomozygous61079803
1214181349214181350GT26GENIChomozygous61079804
1214181352214181353AT26GENIChomozygous61079805
1214181357214181358AT28GENIChomozygous61079806
1214181360214181361AG27GENIChomozygous61079807
1214181361214181362AG27GENIChomozygous61079808
1214181363214181364AG26GENIChomozygous61079809