chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71108679211086793TC33GENIChomozygous68595900
71108788111087882CT28GENIChomozygous71578120
71108897211088973GA26GENIChomozygous71578122
71109480411094805CA52GENICpossibly homozygous68595907
71109558811095589GA49GENIChomozygous68595914
71109604211096043AG37GENIChomozygous70505051
71109796511097966GA37GENIChomozygous68595917
71109856311098564AG40GENICpossibly homozygous68595928
71110022611100227CG19GENIChomozygous68595929
71110148311101484CT10GENICpossibly homozygous68595950
71110156711101568AG11GENIChomozygous68595960
71110157811101579CT10GENIChomozygous68595963
71110337411103375TC7GENICheterozygous68595976
71110050211100503GA29GENICpossibly homozygous69716972
71110187911101880GA22GENIChomozygous69716975
71110170711101708CG16GENIChomozygous69957184