chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5138804296138804297CT17GENICpossibly homozygous670796742
5138804444138804445AG14GENIChomozygous670796743
5138804945138804946AG21GENICheterozygous670796744
5138805141138805142CT17GENICheterozygous670796745
5138806125138806126CA25GENICpossibly homozygous670796746
5138807354138807355AC27GENICpossibly homozygous670796747
5138808474138808476TT--1GENIChomozygous768839300
5138810087138810088AG23GENICpossibly homozygous670796748
5138813044138813045TG4GENIChomozygous670796749
5138813241138813242CCTCTTT1GENIChomozygous768839302
5138813303138813304CT8GENIChomozygous670796750
5138814602138814603CCT2GENIChomozygous768839303