| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130053824-130053983 | Common:1; Rare:68 | ||||
| chr9:130579428-130579698 | Common:7; Rare:106 | ||||
| chr9:130693626-130693806 | Rare:61 | ||||
| chr9:130834646-130834828 | Common:1; Rare:28 | ||||
| chr9:131125419-131125651 | Common:2; Rare:111 | ||||
| chr9:131531182-131531363 | Common:9; Rare:82 | ||||
| chr9:132669661-132669688 | Rare:4 | ||||
| chr9:132669930-132670056 | Common:1; Rare:57 | ||||
| chr9:132878286-132878408 | Common:1; Rare:46 | ||||
| chr9:133030461-133030743 | Common:4; Rare:76 | ||||
| chr9:133336112-133336345 | Common:1; Rare:100 | ||||
| chr9:133348039-133348314 | Common:3; Rare:118 | ||||
| chr9:133356431-133356628 | Common:1; Rare:92; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr9:133375999-133376366 | Common:1; Rare:133 | ||||
| chr9:133417943-133418319 | Common:4; Rare:89 |