| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128724081-128724453 | Common:2; Rare:121 | ||||
| chr9:128881925-128882182 | Common:1; Rare:86 | ||||
| chr9:128947545-128947714 | Common:1; Rare:77; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129835225-129835490 | Common:2; Rare:104 | ||||
| chr9:132878282-132878405 | Common:1; Rare:46 | ||||
| chr9:133030468-133030766 | Common:4; Rare:82 | ||||
| chr9:133348018-133348231 | Common:3; Rare:72 | ||||
| chr9:133356434-133356593 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133417952-133418287 | Common:4; Rare:79 | ||||
| chr9:136410405-136410689 | Common:7; Rare:126 | ||||
| chr9:136944608-136944940 | Common:2; Rare:122 | ||||
| chr9:137188544-137188726 | Common:2; Rare:91 | ||||
| chr9:137205606-137205714 | Rare:40 | ||||
| chr9:137618818-137619026 | Common:1; Rare:93 | ||||
| chrM:2313-2889 |