chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005815610058157TA22GENIChomozygous956126699
141005815810058159TA23GENIChomozygous956126700
141005837210058373AG28GENIChomozygous956126701
141005839310058394AC38GENIChomozygous956126702
141005854510058546CA30GENIChomozygous956126703
141005889610058897GA34GENIChomozygous956126704
141006082010060821AG21GENIChomozygous956126705
141006091510060916TA21GENIChomozygous956126706
141006096610060967CT19GENIChomozygous956126707
141006108710061088GC21GENIChomozygous956126708
141006114010061141CT18GENIChomozygous956126709
141006114210061143AT17GENIChomozygous956126710
141006115310061154TC20GENIChomozygous956126711
141006119810061199GA29GENIChomozygous956126712
141006141410061415AC19GENIChomozygous956126713
141006142010061421GA21GENIChomozygous956126714
141006142310061424TA21GENIChomozygous956126715
141006144610061447CA20GENIChomozygous956126716
141006157910061580AG18GENIChomozygous956126717
141006158510061586AG20GENIChomozygous956126718
141006159510061596GA19GENIChomozygous956126719
141006163110061632CT26GENIChomozygous956126720
141006168610061687TC28GENIChomozygous956126721
141006169310061694AG25GENIChomozygous956126722
141006169410061695AG25GENIChomozygous956126723
141006170010061701CT24GENIChomozygous956126724
141006187310061874GA25GENIChomozygous956126725
141006187510061876CA23GENIChomozygous956126726