chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167089206167089207TC11GENIChomozygous57771879
3167090400167090401AC28GENIChomozygous57771880
3167090527167090528GA20GENIChomozygous57771881
3167091413167091414AG28GENIChomozygous57771882
3167091531167091532AG26GENIChomozygous57771883
3167092039167092040TA32GENIChomozygous57771884
3167093234167093235AT26GENIChomozygous57771885
3167093555167093556TC21GENICpossibly homozygous57771886