chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005837210058373AG19GENIChomozygous942082957
141005839310058394AC25GENIChomozygous942082958
141005854510058546CA28GENIChomozygous942082959
141005889610058897GA26GENIChomozygous942082960
141006082010060821AG26GENIChomozygous942082961
141006091510060916TA17GENIChomozygous942082962
141006096610060967CT23GENIChomozygous942082963
141006108710061088GC26GENIChomozygous942082964
141006114010061141CT17GENIChomozygous942082965
141006114210061143AT17GENIChomozygous942082966
141006115310061154TC22GENIChomozygous942082967
141006119810061199GA30GENIChomozygous942082968
141006141410061415AC21GENIChomozygous942082969
141006142010061421GA20GENIChomozygous942082970
141006142310061424TA22GENIChomozygous942082971
141006144610061447CA26GENIChomozygous942082972
141006157910061580AG29GENIChomozygous942082973
141006158510061586AG31GENIChomozygous942082974
141006159510061596GA32GENIChomozygous942082975
141006163110061632CT32GENIChomozygous942082976
141006168610061687TC27GENIChomozygous942082977
141006169310061694AG28GENIChomozygous942082978
141006169410061695AG28GENIChomozygous942082979
141006170010061701CT27GENIChomozygous942082980
141006187310061874GA25GENIChomozygous942082981
141006187510061876CA26GENIChomozygous942082982