| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128684939-128685098 | Rare:28 | ||||
| chr9:128724089-128724475 | Common:3; Rare:126 | ||||
| chr9:128771877-128772005 | Rare:31 | ||||
| chr9:128787143-128787333 | Common:3; Rare:64 | ||||
| chr9:128881915-128882206 | Common:2; Rare:98 | ||||
| chr9:128921983-128922314 | Common:1; Rare:75 | ||||
| chr9:128947549-128947722 | Common:1; Rare:80; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129110671-129110953 | Common:3; Rare:64 | ||||
| chr9:129111282-129111593 | Common:2; Rare:87 | ||||
| chr9:129139744-129140008 | Rare:51 | ||||
| chr9:129835208-129835486 | Common:2; Rare:113 | ||||
| chr9:130053854-130053935 | Common:1; Rare:26 | ||||
| chr9:130693582-130693800 | Rare:71 | ||||
| chr9:131125437-131125637 | Common:1; Rare:93 | ||||
| chr9:131502869-131503016 | Rare:52; Clinvar:3 |