| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:132406815-132406942 | Rare:43 | ||||
| chr9:132669950-132670051 | Common:1; Rare:48 | ||||
| chr9:132878081-132878412 | Common:2; Rare:131 | ||||
| chr9:133030447-133030742 | Common:4; Rare:78 | ||||
| chr9:133336133-133336314 | Common:1; Rare:74 | ||||
| chr9:133348047-133348258 | Common:2; Rare:84 | ||||
| chr9:133356458-133356593 | Common:1; Rare:61; Clinvar (benign):2 | ||||
| chr9:133376024-133376289 | Common:1; Rare:94 | ||||
| chr9:136410390-136410666 | Common:6; Rare:116 | ||||
| chr9:137188558-137188738 | Common:2; Rare:89 | ||||
| chr9:137205646-137205738 | Rare:38 | ||||
| chr9:137618797-137619031 | Common:1; Rare:105 | ||||
| chrM:3167-3376 | |||||
| chrM:5286-5744 | |||||
| chrM:5823-6288 |