| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132670277-132670518 | Rare:71 | ||||
| chr9:132878272-132878381 | Common:1; Rare:40 | ||||
| chr9:132878818-132878965 | Rare:25 | ||||
| chr9:133030471-133030742 | Common:4; Rare:69 | ||||
| chr9:133129251-133129418 | Common:2; Rare:48 | ||||
| chr9:133275181-133275431 | Common:1; Rare:53 | ||||
| chr9:133348034-133348258 | Common:3; Rare:87 | ||||
| chr9:133356449-133356642 | Common:1; Rare:94; Clinvar (benign):2 | ||||
| chr9:133375947-133376377 | Common:4; Rare:153 | ||||
| chr9:133417939-133418300 | Common:4; Rare:86 | ||||
| chr9:134135296-134135411 | Common:1; Rare:22 | ||||
| chr9:134371768-134371973 | Rare:56 | ||||
| chr9:136410603-136410680 | Rare:40 | ||||
| chr9:136439817-136440141 | Common:1; Rare:102 | ||||
| chr9:136746010-136746172 | Common:1; Rare:38 |