chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71216112412161125GT21GENICpossibly homozygous53790295
71216198712161988TC16GENIChomozygous53790297
71216406712164068GA29GENIChomozygous53790298
71216439612164397TC16GENIChomozygous53790299
71216469212164693TC21GENIChomozygous53790300
71216483012164831TC18GENIChomozygous53790301
71216503812165039CT23GENIChomozygous53790302
71216526012165261GGCC17GENICheterozygous54301765
71216526012165261GGC17GENICheterozygous54301768