| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130693617-130693868 | Common:1; Rare:102 | ||||
| chr9:131125419-131125707 | Common:2; Rare:134 | ||||
| chr9:131502862-131503052 | Rare:70; Clinvar:3 | ||||
| chr9:132161416-132161661 | Rare:49 | ||||
| chr9:132354918-132355347 | Common:5; Rare:142 | ||||
| chr9:132669936-132670046 | Common:1; Rare:53 | ||||
| chr9:132670373-132670527 | Rare:58 | ||||
| chr9:132878275-132878430 | Common:1; Rare:58 | ||||
| chr9:133030442-133030823 | Common:4; Rare:108 | ||||
| chr9:133336079-133336310 | Common:1; Rare:107 | ||||
| chr9:133347984-133348268 | Common:3; Rare:104 | ||||
| chr9:133356272-133356640 | Common:5; Rare:172; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr9:133375935-133376377 | Common:4; Rare:154 | ||||
| chr9:133417867-133418319 | Common:5; Rare:124 | ||||
| chr9:133459945-133460017 | Rare:29 |