chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005815610058157TA28GENIChomozygous962084645
141005815810058159TA26GENIChomozygous962084646
141005837210058373AG25GENIChomozygous962084647
141005839310058394AC28GENIChomozygous962084648
141005854510058546CA35GENIChomozygous962084649
141005889610058897GA26GENIChomozygous962084650
141006082010060821AG20GENIChomozygous962084651
141006091510060916TA28GENIChomozygous962084652
141006096610060967CT27GENIChomozygous962084653
141006108710061088GC17GENIChomozygous962084654
141006114010061141CT14GENIChomozygous962084655
141006114210061143AT14GENIChomozygous962084656
141006115310061154TC14GENIChomozygous962084657
141006119810061199GA20GENIChomozygous962084658
141006141410061415AC21GENIChomozygous962084659
141006142010061421GA20GENIChomozygous962084660
141006142310061424TA20GENIChomozygous962084661
141006144610061447CA21GENIChomozygous962084662
141006157910061580AG28GENIChomozygous962084663
141006158510061586AG28GENIChomozygous962084664
141006159510061596GA27GENIChomozygous962084665
141006163110061632CT26GENIChomozygous962084666
141006168610061687TC30GENIChomozygous962084667
141006169310061694AG28GENIChomozygous962084668
141006169410061695AG28GENIChomozygous962084669
141006170010061701CT28GENIChomozygous962084670
141006187310061874GA26GENIChomozygous962084671
141006187510061876CA27GENIChomozygous962084672