chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121218535121218536AG46GENIChomozygous115858106
7121222839121222840TC46GENICpossibly homozygous115858108
7121223317121223318CT47GENIChomozygous115858110
7121226093121226094AG59GENIChomozygous115858112
7121227221121227222AG35GENIChomozygous115858114
7121227630121227631AC29GENIChomozygous115858116
7121227893121227894CT55GENIChomozygous115858118
7121228581121228582CG39GENICheterozygous115858120
7121228591121228592CG42GENICheterozygous115858122
7121229029121229030AT47GENIChomozygous115858124
7121229582121229583CA58GENIChomozygous115858126
7121231490121231491GC21GENIChomozygous115858128
7121231601121231602AG36GENIChomozygous115858130
7121232042121232043CG59GENICheterozygous115858132
7121232840121232841GA18GENIChomozygous115858134