chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105724070257240703AATTT22GENICpossibly homozygous51461122
105724070257240703AATT22GENICheterozygous53026465
105724095757240959TT--11GENIChomozygous51461123
105724203257242033AG25GENIChomozygous51461124
105724206357242064CT20GENIChomozygous51461125
105724237257242373CCT9GENICpossibly homozygous51461126
105724562057245621GC31GENIChomozygous51461133
105724640957246410T-17GENICpossibly homozygous51461134
105724671157246712TA23GENIChomozygous51461135