chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117269780117269781TC61GENIChomozygous116671278
8117273129117273130GA52GENIChomozygous116671280
8117273611117273612GT58GENIChomozygous116671282
8117274243117274244GA45GENIChomozygous116671284
8117275503117275504CT50GENIChomozygous116671286
8117276119117276120TC68GENIChomozygous116671288
8117277956117277957GA42GENIChomozygous116671290
8117279363117279364CG72GENICpossibly homozygous116671292