Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:114398469-114398672 | Common:2; Rare:53 | ||||
chr9:115023058-115023258 | Common:2; Rare:30 | ||||
chr9:115650204-115650409 | Common:1; Rare:44 | ||||
chr9:115939558-115939619 | Rare:19 | ||||
chr9:120453928-120454015 | Common:1; Rare:23 | ||||
chr9:124353636-124353957 | Common:2; Rare:76 | ||||
chr9:124357291-124357533 | Common:2; Rare:40 | ||||
chr9:124358041-124358417 | Common:1; Rare:62 | ||||
chr9:124358657-124358937 | Rare:71 | ||||
chr9:125237147-125237323 | Common:2; Rare:44 | ||||
chr9:125238729-125239132 | Common:1; Rare:103 | ||||
chr9:125239187-125239527 | Rare:64 | ||||
chr9:128576902-128577129 | Rare:55; Clinvar:1; Clinvar (benign):4 | ||||
chr9:129828146-129828377 | Common:2; Rare:68 | ||||
chr9:131373407-131373671 | Common:1; Rare:58 |