chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116083680116083681CA65GENIChomozygous116668363
8116084552116084553GT54GENIChomozygous116668365
8116085385116085386AG49GENIChomozygous116668367
8116085453116085454CT61GENICpossibly homozygous116668369
8116086576116086577GT51GENIChomozygous116668375
8116086854116086855CT56GENIChomozygous116668377
8116087089116087090TC61GENIChomozygous116668379
8116087510116087511TC61GENIChomozygous116668381
8116087721116087722AG60GENIChomozygous116668383
8116087816116087817TC55GENIChomozygous116668385
8116087834116087835CT45GENIChomozygous116886007
8116087835116087836CT46GENIChomozygous116886009
8116087918116087919AG49GENIChomozygous116668387
8116088428116088429GC52GENICpossibly homozygous116668391
8116088429116088430AC50GENIChomozygous116668393
8116088521116088522TC55GENIChomozygous116668397
8116088911116088912GA51GENIChomozygous116668401
8116089230116089231GT60GENICheterozygous116886011
8116089521116089522AG63GENIChomozygous116668403
8116089701116089702AG43GENIChomozygous116668405
8116089736116089737AG44GENIChomozygous116668407
8116089788116089789CG42GENIChomozygous116668409
8116090259116090260TC56GENIChomozygous116668411
8116090433116090434AT54GENIChomozygous116668413
8116090580116090581TC40GENIChomozygous116668415
8116090856116090857AT58GENIChomozygous116886013
8116091790116091791AG69GENIChomozygous116668419
8116092563116092564GA54GENIChomozygous116668421