chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105974950359749504GT12GENIChomozygous126383381
105974953259749533GT4GENIChomozygous117995655
105974965159749652AG17GENIChomozygous116608663
105974994159749942GA16GENIChomozygous116608665
105975011659750117AG26GENIChomozygous116608667
105975081659750817CT23GENIChomozygous116608669
105975589659755897TA18GENICpossibly homozygous116608677
105975671959756720GA7GENIChomozygous126383382
105975744359757444TC16GENIChomozygous116608679
105975870259758703GA21GENIChomozygous116608681
105975891859758919AG6GENIChomozygous116608683
105975894759758948AG14GENIChomozygous116608685
105976005859760059GA28GENIChomozygous116608687
105976011859760119TA11GENIChomozygous116608689
105976014659760147TC15GENIChomozygous116788954
105976041359760414AT28GENIChomozygous116608691
105976065059760651GC17GENIChomozygous116608693
105976129359761294AG10GENIChomozygous116788955
105977058359770584CA10GENIChomozygous116608701
105976189559761896GT22GENIChomozygous116608695
105976326559763266GA14GENIChomozygous116608697
105976341159763412TC22GENIChomozygous116608699
105977063959770640CA15GENIChomozygous116608703
105977144059771441TC22GENIChomozygous116608705