| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131393777-131394205 | Common:1; Rare:293 | ||||
| chr9:131502832-131503055 | Rare:155; Clinvar:6 | ||||
| chr9:131531147-131531388 | Common:19; Rare:188 | ||||
| chr9:132079862-132079962 | Rare:23 | ||||
| chr9:132354852-132355351 | Common:10; Rare:303 | ||||
| chr9:132406774-132406944 | Common:2; Rare:97 | ||||
| chr9:132669613-132669793 | Rare:49 | ||||
| chr9:132669859-132670121 | Common:2; Rare:185 | ||||
| chr9:132670269-132670747 | Common:2; Rare:232 | ||||
| chr9:132878269-132878422 | Common:2; Rare:114 | ||||
| chr9:132944528-132945130 | Common:2; Rare:367; Clinvar:6; Clinvar (benign):6 | ||||
| chr9:133030438-133030749 | Common:8; Rare:165 | ||||
| chr9:133121166-133121458 | Common:8; Rare:248 | ||||
| chr9:133148734-133148968 | Common:1; Rare:52 | ||||
| chr9:133149166-133149677 | Common:2; Rare:308 |