chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116083680116083681CA40GENIChomozygous116668363
8116083757116083758CG30GENIChomozygous116987970
8116085385116085386AG27GENIChomozygous116668367
8116085453116085454CT25GENIChomozygous116668369
8116086493116086494TG37GENIChomozygous116987971
8116086576116086577GT28GENIChomozygous116668375
8116087089116087090TC24GENIChomozygous116668379
8116087510116087511TC21GENIChomozygous116668381
8116087721116087722AG25GENIChomozygous116668383
8116087816116087817TC30GENIChomozygous116668385
8116087835116087836CT34GENIChomozygous116886009
8116087918116087919AG34GENIChomozygous116668387
8116088428116088429GC24GENIChomozygous116668391
8116088429116088430AC24GENIChomozygous116668393
8116088521116088522TC17GENIChomozygous116668397
8116088911116088912GA18GENIChomozygous116668401
8116089521116089522AG19GENIChomozygous116668403
8116089701116089702AG30GENIChomozygous116668405
8116089736116089737AG28GENIChomozygous116668407
8116089788116089789CG31GENIChomozygous116668409
8116090259116090260TC33GENIChomozygous116668411
8116090433116090434AT29GENIChomozygous116668413
8116090580116090581TC26GENIChomozygous116668415
8116090856116090857AT12GENIChomozygous116886013
8116091790116091791AG25GENIChomozygous116668419
8116092563116092564GA15GENIChomozygous116668421