| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128322394-128322535 | Common:1; Rare:52 | ||||
| chr9:128322751-128322875 | Common:2; Rare:55; Clinvar (benign):5 | ||||
| chr9:128371205-128371383 | Rare:58 | ||||
| chr9:128552413-128552597 | Rare:72; Clinvar:1 | ||||
| chr9:128656652-128656774 | Common:2; Rare:60; Clinvar (pathogenic):1 | ||||
| chr9:128684959-128685098 | Rare:25 | ||||
| chr9:128724056-128724467 | Common:2; Rare:148 | ||||
| chr9:128947593-128947725 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129110646-129110953 | Common:3; Rare:70 | ||||
| chr9:129178237-129178441 | Common:2; Rare:63 | ||||
| chr9:129835214-129835475 | Common:2; Rare:106 | ||||
| chr9:130053854-130053939 | Common:1; Rare:28 | ||||
| chr9:130579437-130579671 | Common:4; Rare:89 | ||||
| chr9:130693637-130693794 | Rare:53 | ||||
| chr9:131125407-131125637 | Common:2; Rare:105 |