chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
64384516043845161AG23GENIChomozygous115376200
64384578743845788TC20GENIChomozygous115376202
64384579943845800TC22GENIChomozygous115376204
64384585543845856CG22GENIChomozygous114778594
64384621043846211AG18GENIChomozygous114778595
64384755643847557GA25GENIChomozygous114778609
64384928843849289GA23GENIChomozygous115458065
64384910543849106AG16GENICheterozygous115458062
64384910943849110AG15GENICheterozygous115458063
64384911343849114AG16GENICheterozygous115458064
64385254943852550GA21GENIChomozygous115458066
64385260243852603GA27GENIChomozygous114778655
64385443743854438GA17GENIChomozygous114778661
64385512743855128TC21GENIChomozygous114778671
64385513043855131TC21GENIChomozygous115458067
64385514843855149TC24GENIChomozygous115458068
64385577443855775TC27GENIChomozygous114778679
64385636743856368GA10GENIChomozygous114778681
64385661343856614GT19GENIChomozygous114778683
64385725043857251AC37GENICheterozygous114778685
64385848743858488TC28GENIChomozygous114778687
64385856543858566CT28GENICpossibly homozygous115458069
64385897843858979AT14GENIChomozygous115458070
64385954643859547TG15GENIChomozygous114778691
64385961143859612CT21GENIChomozygous115458071
64386059543860596AG26GENIChomozygous114778693
64386069143860692CT26GENIChomozygous114778695
64386110043861101TC18GENIChomozygous114778697
64386125343861254TC37GENIChomozygous114778699
64386141143861412GA28GENIChomozygous114778703
64386166443861665CG10GENIChomozygous114778705
64386201143862012GA37GENIChomozygous114778707
64386201543862016TG38GENIChomozygous115458072