chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121218535121218536AG31GENIChomozygous115858106
7121222839121222840TC22GENIChomozygous115858108
7121223317121223318CT22GENIChomozygous115858110
7121226093121226094AG14GENIChomozygous115858112
7121227221121227222AG26GENIChomozygous115858114
7121227630121227631AC6GENIChomozygous115858116
7121227893121227894CT25GENIChomozygous115858118
7121221329121221329AC17GENIChomozygous128512707
7121228566121228566ACAGAC13GENIChomozygous128512708
7121228594121228594ACACAG19GENIChomozygous128512709
7121229029121229030AT32GENIChomozygous115858124
7121229582121229583CA37GENIChomozygous115858126
7121231490121231491GC37GENIChomozygous115858128
7121231601121231602AG28GENIChomozygous115858130
7121232038121232038GTCT8GENIChomozygous134487013
7121232087121232088CT6GENIChomozygous122850915
7121232089121232090CT7GENICheterozygous122850916
7121232840121232841GA12GENIChomozygous115858134