chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005837210058373AG12GENIChomozygous113335912
141005839310058394AC13GENIChomozygous113335914
141005854510058546CA12GENIChomozygous113335916
141005858910058590CT15GENIChomozygous113335918
141006074310060744CT11GENIChomozygous113335926
141005869510058696CT22GENIChomozygous113335920
141005889610058897GA13GENIChomozygous113335922
141005934910059350GA6GENIChomozygous113335924
141006082010060821AG14GENIChomozygous113335928
141006096610060967CT8GENIChomozygous113335930
141006108710061088GC9GENIChomozygous113335932
141006114010061141CT15GENIChomozygous113335934
141006114210061143AT15GENIChomozygous113335936
141006115310061154TC15GENIChomozygous113335938
141006119810061199GA12GENIChomozygous113335939
141006141410061415AC6GENIChomozygous113335941
141006142010061421GA6GENIChomozygous113335943
141006142310061424TA6GENIChomozygous113335945
141006144610061447CA8GENIChomozygous113335947
141006157910061580AG16GENIChomozygous113335948
141006158510061586AG16GENIChomozygous113335950
141006159510061596GA16GENIChomozygous113335952
141006163110061632CT12GENIChomozygous113335954
141006168610061687TC10GENIChomozygous113335956
141006169310061694AG9GENIChomozygous113335958
141006169410061695AG8GENIChomozygous113335960
141006170010061701CT7GENIChomozygous113335962
141006187310061874GA17GENIChomozygous113335964
141006187510061876CA18GENIChomozygous113335966