chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71108679211086793TC7GENIChomozygous68595900
71108788111087882CT12GENIChomozygous71578120
71108897211088973GA4GENIChomozygous71578122
71109480411094805CA8GENIChomozygous68595907
71109558811095589GA4GENIChomozygous68595914
71109796511097966GA17GENICpossibly homozygous68595917
71109856311098564AG14GENIChomozygous68595928
71109604211096043AG8GENIChomozygous70505051
71110022611100227CG7GENIChomozygous68595929
71110050211100503GA11GENIChomozygous69716972
71110148311101484CT3GENIChomozygous68595950
71110156711101568AG3GENIChomozygous68595960
71110157811101579CT4GENIChomozygous68595963
71110187911101880GA4GENIChomozygous69716975