chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2314857223148573GA14GENIChomozygous108544943
X2314922623149227GA15GENIChomozygous108544944
X2314928423149285TG9GENIChomozygous108544946
X2314956023149561CT7GENIChomozygous108544948
X2314981123149812GA14GENIChomozygous108544950
X2314996923149970GA17GENIChomozygous108544952
X2315090123150902CT9GENIChomozygous108544954
X2315167723151678AG13GENIChomozygous108239673
X2315301823153019TC12GENIChomozygous108373206
X2315308023153081TG11GENICheterozygous108373208
X2315385323153854AC15GENIChomozygous108239681
X2315449323154494CA5GENIChomozygous108544956
X2316193623161937CT10GENIChomozygous108544960
X2316218223162183CT22GENIChomozygous108544962
X2316249523162496CT18GENIChomozygous108544964
X2316251123162512AG20GENIChomozygous108544966
X2316280423162805TC12GENIChomozygous108239687
X2316374523163746GA11GENIChomozygous108239693
X2316375823163759AG12GENIChomozygous108239695
X2316428823164289TC22GENIChomozygous108239699
X2316502323165024CA14GENIChomozygous108544968
X2316505823165059CT11GENIChomozygous108544970
X2316523323165234GA10GENIChomozygous108544972
X2316531623165317TC21GENIChomozygous108239701
X2316563623165637AT11GENIChomozygous108544974
X2315301923153020GA12GENIChomozygous108701204
X2316179023161791GA3GENIChomozygous108701206