chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120889180120889181CT27GENIChomozygous54085079
7120892430120892431CT15GENIChomozygous54085083
7120892769120892770GA32GENIChomozygous54085084
7120893276120893277GA17GENIChomozygous54085085
7120893284120893285CT18GENIChomozygous54085086
7120893574120893575GA13GENICpossibly homozygous54085087
7120893824120893825CA13GENICpossibly homozygous54085088
7120893886120893887TTC3GENIChomozygous54085089
7120892046120892049AAC---3GENICheterozygous54921146
7120892058120892059CCAA3GENICheterozygous54921148