chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
389829848982985GA49GENIChomozygous774585704
389835598983560CT38GENIChomozygous774585705
389836258983626CG52GENIChomozygous774585706
389842678984268TA59GENIChomozygous774585707
389843058984306TA51GENIChomozygous774585708
389850278985028AG36GENIChomozygous774585709
389855888985589GT14GENIChomozygous774585710
389869088986909GA35GENICheterozygous774585711
389872988987299CT21GENICheterozygous774585712
389873468987347CG15GENIChomozygous774585713
389873688987369AC13GENIChomozygous774585714
389873728987373CG12GENIChomozygous774585715
389876288987629CA9GENICheterozygous774585716
389876808987681CA9GENICpossibly homozygous774585717
389879148987915CG4GENIChomozygous774585718
389879188987919CG4GENICheterozygous774585719
389883348988335CG16GENIChomozygous774585720
389893458989346TC32GENIChomozygous774585721
389906338990634TC49GENIChomozygous774585722
389923788992379AG46GENIChomozygous774585723
389926378992638AG68GENIChomozygous774585724
389948468994847GA54GENIChomozygous774585725
389973408997341AG15GENIChomozygous774585726
389982298998230GA36GENICpossibly homozygous774585727
389984358998436TC46GENIChomozygous774585728
390029759002976CT70GENIChomozygous774585729
390034199003420GA53GENIChomozygous774585730
390049659004966TG42GENICpossibly homozygous774585731
390056899005690GA41GENIChomozygous774585732
390065329006533TC39GENIChomozygous774585733
390068469006847TC44GENIChomozygous774585734
390078889007889CT40GENIChomozygous774585735
390087439008744CT56GENIChomozygous774585736
390094699009470AG50GENIChomozygous774585737
390096289009629TC67GENIChomozygous774585738
390107119010712CT35GENICpossibly homozygous774585739
390111229011123GA55GENIChomozygous774585740
390116659011666TG30GENICheterozygous774585741