chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105724070257240703AATTT19GENIChomozygous51461122
105724095757240959TT--18GENICpossibly homozygous51461123
105724095857240959T-18GENICheterozygous51893383
105724203257242033AG30GENIChomozygous51461124
105724206357242064CT27GENIChomozygous51461125
105724237257242373CCT20GENIChomozygous51461126
105724562057245621GC30GENIChomozygous51461133
105724640957246410T-24GENICpossibly homozygous51461134
105724671157246712TA31GENIChomozygous51461135