chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3167089206167089207TC19GENIChomozygous57771879
3167090400167090401AC18GENIChomozygous57771880
3167090527167090528GA18GENIChomozygous57771881
3167091413167091414AG21GENICpossibly homozygous57771882
3167091531167091532AG26GENICpossibly homozygous57771883
3167092039167092040TA26GENICpossibly homozygous57771884
3167093234167093235AT22GENIChomozygous57771885
3167093555167093556TC20GENIChomozygous57771886