chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
149189635491896355TC8GENIChomozygous114101878
149189747591897476CT18GENIChomozygous114101879
149189823991898240AG14GENIChomozygous114101880
149190000591900006AC10GENIChomozygous114101881
149190151491901515GT29GENICpossibly homozygous114101882
149190347791903478AG10GENIChomozygous114101884