chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116083680116083681CA42GENIChomozygous116668363
8116083757116083758CG42GENIChomozygous116987970
8116085385116085386AG25GENIChomozygous116668367
8116085453116085454CT21GENIChomozygous116668369
8116086493116086494TG28GENIChomozygous116987971
8116086576116086577GT27GENIChomozygous116668375
8116087089116087090TC25GENIChomozygous116668379
8116087510116087511TC26GENIChomozygous116668381
8116087721116087722AG32GENIChomozygous116668383
8116087816116087817TC43GENIChomozygous116668385
8116087835116087836CT45GENIChomozygous116886009
8116087918116087919AG30GENIChomozygous116668387
8116088428116088429GC32GENIChomozygous116668391
8116088429116088430AC32GENIChomozygous116668393
8116088521116088522TC37GENIChomozygous116668397
8116088911116088912GA25GENIChomozygous116668401
8116089521116089522AG23GENIChomozygous116668403
8116089701116089702AG17GENIChomozygous116668405
8116089736116089737AG19GENIChomozygous116668407
8116089788116089789CG28GENIChomozygous116668409
8116090259116090260TC21GENIChomozygous116668411
8116090433116090434AT28GENIChomozygous116668413
8116090580116090581TC26GENIChomozygous116668415
8116090856116090857AT35GENIChomozygous116886013
8116091790116091791AG32GENIChomozygous116668419
8116092563116092564GA21GENIChomozygous116668421