chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116083187116083188GA17GENIChomozygous116668359
8116083295116083296GA19GENIChomozygous116668361
8116084552116084553GT29GENIChomozygous116668365
8116085385116085386AG12GENIChomozygous116668367
8116085453116085454CT15GENIChomozygous116668369
8116085630116085631GA21GENIChomozygous116668371
8116085942116085943CT28GENIChomozygous116668373
8116086576116086577GT20GENIChomozygous116668375
8116087089116087090TC16GENIChomozygous116668379
8116087510116087511TC19GENIChomozygous116668381
8116087721116087722AG25GENIChomozygous116668383
8116087816116087817TC14GENIChomozygous116668385
8116087918116087919AG13GENIChomozygous116668387
8116088288116088289CT19GENIChomozygous116668389
8116088428116088429GC17GENIChomozygous116668391
8116088429116088430AC17GENIChomozygous116668393
8116088488116088489CT20GENIChomozygous116668395
8116088521116088522TC18GENIChomozygous116668397
8116088833116088834CT23GENIChomozygous116668399
8116088911116088912GA22GENIChomozygous116668401
8116089521116089522AG13GENIChomozygous116668403
8116089701116089702AG27GENIChomozygous116668405
8116089736116089737AG26GENICpossibly homozygous116668407
8116089788116089789CG24GENIChomozygous116668409
8116090259116090260TC21GENIChomozygous116668411
8116090433116090434AT20GENIChomozygous116668413
8116090580116090581TC30GENIChomozygous116668415
8116091424116091425GC20GENIChomozygous116668417
8116091790116091791AG21GENIChomozygous116668419
8116092563116092564GA5GENIChomozygous116668421