chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X6537101465371015TA5GENIChomozygous805578667
X6537316665373167GA20GENIChomozygous805578668
X6537418565374186GA12GENIChomozygous805578669
X6537590465375905AG10GENIChomozygous805578670
X6537672765376728GA6GENIChomozygous805578671
X6538225165382252TA13GENIChomozygous805578672
X6538315765383158TC5GENIChomozygous805578673
X6538465365384654TC2GENIChomozygous805578674
X6538505665385057CT5GENIChomozygous805578675
X6538910265389103GA17GENICheterozygous805578676
X6539017065390171AG10GENIChomozygous805578677
X6539077265390773TA12GENICheterozygous805578678
X6539077965390780GT18GENICheterozygous805578679
X6539086965390870AG55GENICheterozygous805578680
X6539087065390871CG58GENICheterozygous805578681
X6539092965390930CT44GENICheterozygous805578682
X6539102565391026TC11GENICheterozygous805578683
X6539159865391599GA12GENICheterozygous805578684
X6539165665391657CT10GENICheterozygous805578685
X6539205365392054AC13GENIChomozygous805578686
X6539221065392211GA8GENIChomozygous805578687
X6539395665393957GA13GENIChomozygous805578688
X6539424765394248AT12GENICpossibly homozygous805578689
X6539426865394269TA12GENICpossibly homozygous805578690
X6539496265394963GA18GENICheterozygous805578691
X6539503865395039AG15GENICheterozygous805578692
X6539555965395560TA31GENICheterozygous805578693
X6539825765398258AG3GENIChomozygous805578694
X6539894165398942TC5GENIChomozygous805578695