chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46908892869088929GC15GENICpossibly homozygous70798644
46908897469088975CG15GENICheterozygous71538457
46908897669088977CG15GENICheterozygous71538459
46908897869088979CG15GENICheterozygous71538461
46908946569089466GA35GENIChomozygous70798653
46908980669089807GA29GENIChomozygous70798656
46908988869089889CA49GENICpossibly homozygous70798659
46908988969089890CG49GENIChomozygous70798662
46909011269090113AG44GENIChomozygous70798665
46909025269090253CA25GENIChomozygous70798668
46909054969090550GA43GENIChomozygous70798671
46909104369091044GT18GENIChomozygous70798674
46909140769091408GA23GENIChomozygous70798677
46909218569092186CT55GENICpossibly homozygous70798680
46909299969093000TA35GENIChomozygous70798683