chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005815610058157TA24GENIChomozygous959103677
141005837210058373AG23GENIChomozygous959103678
141005839310058394AC25GENIChomozygous959103679
141005854510058546CA24GENIChomozygous959103680
141005889610058897GA28GENIChomozygous959103681
141006082010060821AG20GENIChomozygous959103682
141006091510060916TA14GENIChomozygous959103683
141006096610060967CT14GENIChomozygous959103684
141006108710061088GC14GENIChomozygous959103685
141006114010061141CT14GENIChomozygous959103686
141006114210061143AT14GENIChomozygous959103687
141006115310061154TC17GENIChomozygous959103688
141006119810061199GA23GENIChomozygous959103689
141006141410061415AC29GENIChomozygous959103690
141006142010061421GA25GENIChomozygous959103691
141006142310061424TA24GENIChomozygous959103692
141006144610061447CA31GENIChomozygous959103693
141006157910061580AG36GENIChomozygous959103694
141006158510061586AG31GENIChomozygous959103695
141006159510061596GA34GENIChomozygous959103696
141006163110061632CT34GENIChomozygous959103697
141006168610061687TC25GENIChomozygous959103698
141006169310061694AG26GENIChomozygous959103699
141006169410061695AG27GENIChomozygous959103700
141006170010061701CT27GENIChomozygous959103701
141006187310061874GA28GENIChomozygous959103702
141006187510061876CA29GENIChomozygous959103703