chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105523942155239422TC51GENIChomozygous142249074
105524034255240343TC47GENICpossibly homozygous142249075
105524044355240444CT55GENIChomozygous142249076
105524064955240650CG29GENICheterozygous154651003
105524064955240650C29GENICpossibly homozygous403287019
105524065355240654C29GENICpossibly homozygous403287020
105524065355240654CG29GENICheterozygous403287021
105524065755240658C38GENICheterozygous403287022
105524066555240666CG37GENIChomozygous142249077
105524066155240662C37GENICheterozygous403634920
105524065755240658CG38GENIChomozygous138793387
105524066155240662CG37GENIChomozygous138793388