chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121218535121218536AG18GENIChomozygous115858106
7121222839121222840TC19GENIChomozygous115858108
7121223317121223318CT21GENIChomozygous115858110
7121226093121226094AG25GENIChomozygous115858112
7121227221121227222AG28GENIChomozygous115858114
7121227630121227631AC11GENIChomozygous115858116
7121227893121227894CT29GENIChomozygous115858118
7121229029121229030AT16GENIChomozygous115858124
7121229582121229583CA26GENIChomozygous115858126
7121231490121231491GC30GENIChomozygous115858128
7121231601121231602AG22GENIChomozygous115858130
7121221329121221329AC32GENIChomozygous128512707
7121228566121228566ACAGAC7GENIChomozygous128512708
7121228594121228594ACACAG13GENICpossibly homozygous128512709
7121232041121232041TG6GENICheterozygous128512711
7121232087121232088CT7GENIChomozygous122850915
7121232840121232841GA15GENIChomozygous115858134