chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71216112412161125GT30GENIChomozygous53790295
71216198712161988TC28GENIChomozygous53790297
71216406712164068GA27GENIChomozygous53790298
71216439612164397TC38GENIChomozygous53790299
71216469212164693TC22GENIChomozygous53790300
71216483012164831TC30GENIChomozygous53790301
71216503812165039CT34GENIChomozygous53790302
71216526012165261GGCC31GENICheterozygous54301765
71216526012165261GGC31GENICpossibly homozygous54301768