chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191147414411474145TC13GENIChomozygous109636727
191148047411480475AG28GENIChomozygous109636731
191148094011480941AG25GENIChomozygous109636733
191148313011483131CA32GENIChomozygous109636735
191148454311484544AG22GENIChomozygous109636737
191148521311485214CG25GENIChomozygous109636739
191148626311486264AG25GENIChomozygous109636741
191148629511486296CT20GENIChomozygous109636743
191149562611495627AT21GENIChomozygous109636761
191149653011496531CT29GENIChomozygous109636763
191149738311497384CT22GENIChomozygous109636765
191149867911498680AC30GENIChomozygous109636769
191149980011499801GT21GENICpossibly homozygous109636771
191150134311501344CT11GENIChomozygous109995452
191147848711478488GA14GENIChomozygous109995441
191149155811491559AT28GENIChomozygous109995448
191150203911502040GC15GENIChomozygous109995454
191150231611502317GA19GENIChomozygous109995457
191150254811502549CA27GENIChomozygous109636775
191150317911503180GT38GENIChomozygous109995459
191150437811504379GT29GENIChomozygous109636777
191150446011504461CT27GENIChomozygous109995461
191150509911505100AG30GENIChomozygous109636781
191150564911505650TC16GENIChomozygous109636785
191150620311506204AG18GENIChomozygous109636795
191150624011506241AG20GENIChomozygous109995463
191150681511506816CT23GENIChomozygous109995465
191150838511508386CT5GENIChomozygous109995467