chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5104985774104985775GT33GENIChomozygous55617359
5104986174104986180ACACAC------14GENIChomozygous55617360
5104989729104989730A-27GENIChomozygous55617362
5104991452104991453AAAATC21GENIChomozygous55617363
5104992805104992806TTA23GENICpossibly homozygous55617364
5104993722104993723AG16GENIChomozygous55617365
5104998162104998164AG--10GENICheterozygous56439581
5105002729105002730C-4GENIChomozygous56439604
5105005288105005289GA17GENIChomozygous55617369
5105005512105005513GC36INTERGENIChomozygous55617370
5105006607105006608AATCTCTCTCTCTCTC8INTERGENICpossibly homozygous56491357
5105006607105006608AATCTCTCTC8INTERGENICheterozygous56717415
5105006654105006666GTGTGTGTGTGT------------3INTERGENIChomozygous56491359