| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:123999069-123999245 | Common:3; Rare:30 | ||||
| chr9:124000078-124000233 | Common:2; Rare:45 | ||||
| chr9:124009346-124009563 | Common:1; Rare:39 | ||||
| chr9:124658258-124658443 | Rare:36 | ||||
| chr9:128220044-128220219 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr9:129258433-129258671 | Common:3; Rare:55 | ||||
| chr9:129320800-129321058 | Rare:56 | ||||
| chr9:129336653-129336927 | Common:2; Rare:53 | ||||
| chr9:129413749-129413949 | Common:3; Rare:84 | ||||
| chr9:130712677-130712858 | Common:2; Rare:59 | ||||
| chr9:131373427-131373709 | Common:1; Rare:70 | ||||
| chr9:133144563-133144676 | Common:4; Rare:30 | ||||
| chr9:133609166-133609472 | Common:2; Rare:84 | ||||
| chr9:135480727-135480815 | Rare:19 | ||||
| chr9:136400137-136400319 | Common:2; Rare:61 |