chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005437210054373AC15INTERGENIChomozygous786805074
141005587110055872GA12INTERGENIChomozygous786805075
141005799910058000TC8INTERGENIChomozygous786805076
141005837210058373AG30INTERGENIChomozygous786805077
141005839310058394AC23INTERGENIChomozygous786805078
141005854510058546CA29INTERGENICpossibly homozygous786805079
141005858910058590CT27INTERGENIChomozygous786805080
141005869510058696CT28INTERGENIChomozygous786805081
141005889610058897GA25INTERGENIChomozygous786805082
141005934910059350GA18INTERGENIChomozygous786805083
141006074310060744CT22GENIChomozygous786805084
141006082010060821AG36GENIChomozygous786805085
141006096610060967CT25GENIChomozygous786805086
141006108710061088GC29GENIChomozygous786805087
141006114010061141CT17GENIChomozygous786805088
141006114210061143AT17GENIChomozygous786805089
141006115310061154TC17GENIChomozygous786805090
141006119810061199GA22GENIChomozygous786805091
141006131410061315AG31GENICheterozygous786805092
141006141410061415AC34GENIChomozygous786805093
141006142010061421GA29GENIChomozygous786805094
141006142310061424TA27GENIChomozygous786805095
141006144610061447CA31GENIChomozygous786805096
141006157910061580AG24GENIChomozygous786805097
141006158510061586AG28GENIChomozygous786805098
141006159510061596GA30GENIChomozygous786805099
141006163110061632CT25GENIChomozygous786805100
141006168610061687TC29GENIChomozygous786805101
141006169310061694AG25GENIChomozygous786805102
141006169410061695AG25GENIChomozygous786805103
141006170010061701CT27GENIChomozygous786805104
141006187310061874GA23GENIChomozygous786805105
141006187510061876CA22GENIChomozygous786805106