chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71108679211086793TC25GENIChomozygous68595900
71108788111087882CT24GENIChomozygous71578120
71108897211088973GA23GENIChomozygous71578122
71109480411094805CA44GENIChomozygous68595907
71109558811095589GA33GENIChomozygous68595914
71109796511097966GA30GENIChomozygous68595917
71109856311098564AG49GENIChomozygous68595928
71110022611100227CG19GENIChomozygous68595929
71109604211096043AG37GENIChomozygous70505051
71110050211100503GA29GENIChomozygous69716972
71110148311101484CT4GENIChomozygous68595950
71110156711101568AG11GENIChomozygous68595960
71110157811101579CT9GENIChomozygous68595963
71110187911101880GA24GENIChomozygous69716975
71110170711101708CG17GENICpossibly homozygous69957184