chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
187670448776704488CT6GENIChomozygous110409736
187670499176704992AG7GENIChomozygous110409740
187670505376705054AG10GENIChomozygous110409742
187670512176705122AG18GENIChomozygous125361378
187670515176705152GT14GENIChomozygous125361380
187670562376705624AG22GENIChomozygous110409746
187670579976705800CT12GENIChomozygous110409748
187670682076706821TC9GENIChomozygous110409749
187670712776707128TC14GENIChomozygous110409751
187670723476707235GA9GENIChomozygous110409753
187670765876707659TC7GENIChomozygous110409759
187670804376708044AG13GENIChomozygous110409761
187670807076708071AG22GENIChomozygous110409763
187670900976709010TC8GENIChomozygous110409767
187670901876709019TC9GENIChomozygous110409769
187670904676709047TG12GENIChomozygous110409771
187670915376709154GA6GENIChomozygous110409773
187670915776709158GA8GENIChomozygous110409775
187670918676709187CT13GENIChomozygous110409777
187670829276708293AG13GENIChomozygous110870245
187671006876710069GA14GENIChomozygous110409785
187671013276710133AG10GENIChomozygous110409787
187671016276710163TC6GENIChomozygous110409789
187671017576710176CT4GENIChomozygous110409791
187671042076710421AG8GENIChomozygous110409793
187671053176710532AG7GENIChomozygous110409797
187671130176711302CA10GENIChomozygous110409799
187670795376707954CT16GENIChomozygous110733119
187670823776708238CT20GENIChomozygous110733121
187670873776708738GA12GENIChomozygous110733123
187671047376710474CT10GENIChomozygous110733125
187671267576712676GA21GENIChomozygous110409801
187671281076712811CT17GENIChomozygous110409803
187671291876712919GC21GENIChomozygous110409804
187671233476712335AT17GENIChomozygous119502361