chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5104985774104985775GT2GENIChomozygous55617359
5104986174104986180ACACAC------2GENIChomozygous55617360
5104989729104989730A-2GENIChomozygous55617362
5104991452104991453AAAATC3GENIChomozygous55617363
5104992805104992806TTA7GENICpossibly homozygous55617364
5104993722104993723AG19GENIChomozygous55617365
5105002729105002730C-1GENIChomozygous56439604
5105005288105005289GA23GENIChomozygous55617369
5105005512105005513GC23INTERGENICpossibly homozygous55617370