chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96770038767700388CA50GENIChomozygous794910725
96770151367701514GT41GENIChomozygous794910726
96770223567702236CT49GENIChomozygous794910727
96770244167702442CT41GENIChomozygous794910728
96770262767702628GA22GENIChomozygous794910729
96770267667702677CT30GENIChomozygous794910730
96770302267703023TC34GENICpossibly homozygous794910731
96770320467703205AC53GENIChomozygous794910732
96770332167703322AG61GENIChomozygous794910733
96770377167703772GA34GENIChomozygous794910734
96770384667703847GC33GENIChomozygous794910735
96770391767703918CT30GENICpossibly homozygous794910736