chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105661033756610338GA38GENIChomozygous116935517
105661166956611670GA30GENIChomozygous116935519
105661205856612059AG17GENIChomozygous116935521
105661262056612621CT17GENICpossibly homozygous118074938
105661271756612718AG36GENIChomozygous116935523
105661325956613260AG35GENIChomozygous116935525
105661455556614556CT46GENIChomozygous116935527
105661545356615454TC30GENIChomozygous116935529
105661558256615583TC29GENIChomozygous116935531
105661771256617713AG33GENIChomozygous116935533
105661775456617755CT29GENIChomozygous116935535
105661827256618273TC32GENIChomozygous116935537