chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005837210058373AG28GENIChomozygous983311098
141005839310058394AC27GENIChomozygous983311099
141005854510058546CA24GENIChomozygous983311100
141005858910058590CT31GENIChomozygous983311101
141005869510058696CT21GENIChomozygous983311102
141005889610058897GA16GENIChomozygous983311103
141005934910059350GA12GENIChomozygous983311104
141006074310060744CT17GENIChomozygous983311105
141006082010060821AG11GENIChomozygous983311106
141006096610060967CT21GENIChomozygous983311107
141006108710061088GC20GENIChomozygous983311108
141006114010061141CT13GENIChomozygous983311109
141006114210061143AT13GENIChomozygous983311110
141006115310061154TC14GENIChomozygous983311111
141006119810061199GA15GENIChomozygous983311112
141006141410061415AC22GENICpossibly homozygous983311113
141006142010061421GA18GENIChomozygous983311114
141006142310061424TA17GENIChomozygous983311115
141006144610061447CA15GENIChomozygous983311116
141006157910061580AG32GENIChomozygous983311117
141006158510061586AG29GENIChomozygous983311118
141006159510061596GA28GENIChomozygous983311119
141006163110061632CT27GENIChomozygous983311120
141006168610061687TC25GENIChomozygous983311121
141006169310061694AG25GENIChomozygous983311122
141006169410061695AG24GENIChomozygous983311123
141006170010061701CT22GENIChomozygous983311124
141006187310061874GA25GENIChomozygous983311125
141006187510061876CA23GENIChomozygous983311126