chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4205128834205128835GA24GENIChomozygous652172677
4205129264205129265AG24GENIChomozygous652172678
4205129586205129587TTG16GENIChomozygous758341265
4205129782205129783TC20GENIChomozygous652172679
4205129956205129957CT22GENIChomozygous652172680
4205130242205130243CT27GENIChomozygous652172681
4205130304205130305CT20GENIChomozygous652172682
4205130305205130306TC20GENIChomozygous652172683
4205130578205130579CT24GENIChomozygous652172684
4205130927205130928CG29GENIChomozygous652172685
4205131056205131057TC23GENIChomozygous652172686
4205131067205131068AG23GENIChomozygous652172687
4205131439205131440GC20GENIChomozygous652172688
4205132645205132646GA20GENIChomozygous652172689
4205133026205133027GA21GENIChomozygous652172690
4205133039205133040AG17GENIChomozygous652172691
4205133447205133448GA24GENIChomozygous652172692
4205133966205133967CT17GENIChomozygous652172693
4205134011205134012TC28GENIChomozygous652172694
4205134854205134855CT18GENIChomozygous652172695
4205135577205135578CT27GENIChomozygous652172696
4205138221205138222TC13GENIChomozygous652172697
4205138227205138228GGTT11GENICpossibly homozygous758341266
4205138227205138228GGTTT11GENICheterozygous758341267
4205149823205149824TC16GENIChomozygous652172698
4205149920205149921TA18GENIChomozygous652172699