chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46908913269089133CT26GENIChomozygous71990772
46908988869089889CA17GENIChomozygous70798659
46908988969089890CG16GENIChomozygous70798662
46909011269090113AG18GENIChomozygous70798665
46909025269090253CA25GENIChomozygous70798668
46909104369091044GT22GENIChomozygous70798674
46909215069092151TC22GENIChomozygous71990774
46909216369092164AG27GENICpossibly homozygous71990776