| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128881901-128882197 | Common:2; Rare:96 | ||||
| chr9:128921983-128922347 | Common:2; Rare:86 | ||||
| chr9:128947593-128947721 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129110612-129110949 | Common:3; Rare:75 | ||||
| chr9:129141576-129141673 | Common:2; Rare:29 | ||||
| chr9:129835218-129835492 | Common:2; Rare:110 | ||||
| chr9:130043086-130043334 | Common:2; Rare:85 | ||||
| chr9:130053874-130053979 | Common:1; Rare:48 | ||||
| chr9:130693626-130693794 | Rare:53 | ||||
| chr9:131502869-131503016 | Rare:52; Clinvar:3 | ||||
| chr9:131531171-131531363 | Common:9; Rare:87 | ||||
| chr9:132354955-132355274 | Common:5; Rare:103 | ||||
| chr9:132406807-132406870 | Rare:21 | ||||
| chr9:132669950-132670051 | Common:1; Rare:48 | ||||
| chr9:132878308-132878374 | Common:1; Rare:20 |