chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187670471576704716TC11GENIChomozygous110409738
187670505376705054AG11GENIChomozygous110409742
187670533676705337TC11GENIChomozygous110409744
187670562376705624AG25GENIChomozygous110409746
187670579976705800CT12GENIChomozygous110409748
187670682076706821TC19GENIChomozygous110409749
187670712776707128TC18GENIChomozygous110409751
187670723476707235GA19GENIChomozygous110409753
187670738776707388TC18GENIChomozygous110409755
187670760976707610AG11GENIChomozygous110409757
187670765876707659TC13GENIChomozygous110409759
187670804376708044AG14GENIChomozygous110409761
187670807076708071AG22GENIChomozygous110409763
187670898276708983TC16GENIChomozygous110409765
187670900976709010TC16GENIChomozygous110409767
187670901876709019TC20GENIChomozygous110409769
187670904676709047TG18GENIChomozygous110409771
187670915376709154GA19GENIChomozygous110409773
187670915776709158GA18GENIChomozygous110409775
187670918676709187CT22GENIChomozygous110409777
187670953476709535GA10GENIChomozygous110409779
187670994276709943GA6GENIChomozygous110409783
187671006876710069GA21GENIChomozygous110409785
187671013276710133AG16GENIChomozygous110409787
187671016276710163TC14GENIChomozygous110409789
187671017576710176CT11GENIChomozygous110409791
187671042076710421AG16GENIChomozygous110409793
187671044776710448AG18GENIChomozygous110409795
187670823776708238CT26GENIChomozygous110733121
187671053176710532AG18GENIChomozygous110409797
187671130176711302CA29GENIChomozygous110409799
187671267576712676GA21GENIChomozygous110409801
187671291876712919GC31GENIChomozygous110409804
187671353776713538CT13GENIChomozygous110409806
187671366076713661TA14GENIChomozygous110409808
187671437476714375AG6GENIChomozygous110409810