chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4118241097118241098AT20GENIChomozygous112821720
4118241862118241863CT17GENIChomozygous113153609
4118242641118242642AG17GENIChomozygous112821722
4118243624118243625AG19GENIChomozygous113153610
4118244710118244711TC29GENIChomozygous113153611
4118244850118244851AG25GENIChomozygous112821726
4118244938118244939CT27GENIChomozygous113153612
4118245852118245853AG39GENIChomozygous112821728
4118246529118246530TG19GENIChomozygous113153613
4118246729118246730AG26GENIChomozygous112821730
4118247048118247049GA23GENIChomozygous113153614
4118247081118247082GA22GENIChomozygous113153615
4118250259118250260CT27GENIChomozygous113153616
4118250671118250672TC12GENIChomozygous113153617
4118254632118254633AG20GENIChomozygous113153618
4118255057118255058GC22GENIChomozygous112821734
4118256467118256468CT21GENIChomozygous113153619
4118256600118256601TC23GENIChomozygous112821736
4118256728118256729TA24GENICpossibly homozygous113153620
4118257746118257747TC12GENIChomozygous113153621
4118259196118259197TG22GENIChomozygous112821738
4118260242118260243AG17GENICpossibly homozygous113153622
4118261717118261718GA18GENIChomozygous113153623
4118261893118261894GA19GENIChomozygous113153624
4118262663118262664TG34GENIChomozygous113153625
4118263329118263330AC36GENIChomozygous113153626
4118265673118265674AG24GENIChomozygous113153627
4118267193118267194TG24GENIChomozygous112821740
4118267623118267624AC26GENIChomozygous113153628
4118268504118268505TC17GENIChomozygous113153629
4118269501118269502TC25GENIChomozygous112821744
4118270051118270052AT26GENIChomozygous113153630
4118270396118270397GA19GENIChomozygous113153631
4118270954118270955TC21GENIChomozygous113153632