chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005837210058373AG12GENIChomozygous933221691
141005839310058394AC13GENIChomozygous933221692
141005854510058546CA12GENIChomozygous933221693
141005858910058590CT15GENIChomozygous933221694
141005869510058696CT22GENIChomozygous933221695
141005889610058897GA13GENIChomozygous933221696
141005934910059350GA6GENIChomozygous933221697
141006074310060744CT11GENIChomozygous933221698
141006082010060821AG14GENIChomozygous933221699
141006096610060967CT8GENIChomozygous933221700
141006108710061088GC9GENIChomozygous933221701
141006114010061141CT15GENIChomozygous933221702
141006114210061143AT15GENIChomozygous933221703
141006115310061154TC15GENIChomozygous933221704
141006119810061199GA12GENIChomozygous933221705
141006141410061415AC6GENIChomozygous933221706
141006142010061421GA6GENIChomozygous933221707
141006142310061424TA6GENIChomozygous933221708
141006144610061447CA8GENIChomozygous933221709
141006157910061580AG16GENIChomozygous933221710
141006158510061586AG16GENIChomozygous933221711
141006159510061596GA16GENIChomozygous933221712
141006163110061632CT12GENIChomozygous933221713
141006168610061687TC10GENIChomozygous933221714
141006169310061694AG9GENIChomozygous933221715
141006169410061695AG8GENIChomozygous933221716
141006170010061701CT7GENIChomozygous933221717
141006187310061874GA17GENIChomozygous933221718
141006187510061876CA18GENIChomozygous933221719