chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5104985774104985775GT24GENIChomozygous55617359
5104985942104985943AAAAGG9GENICpossibly homozygous56491356
5104986174104986180ACACAC------19GENIChomozygous55617360
5104989729104989730A-27GENIChomozygous55617362
5104991452104991453AAAATC28GENIChomozygous55617363
5104992805104992806TTA28GENIChomozygous55617364
5104993722104993723AG14GENIChomozygous55617365
5105002729105002730C-11GENICpossibly homozygous56439604
5105005288105005289GA15GENIChomozygous55617369
5105005512105005513GC29INTERGENIChomozygous55617370
5105006652105006666GTGTGTGTGTGTGT--------------14INTERGENICheterozygous56491358
5105006654105006666GTGTGTGTGTGT------------14INTERGENICheterozygous56491359