| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130053847-130053939 | Common:1; Rare:30 | ||||
| chr9:130693600-130693808 | Rare:73 | ||||
| chr9:131096236-131096588 | Common:4; Rare:95 | ||||
| chr9:131125425-131125637 | Common:2; Rare:98 | ||||
| chr9:131531182-131531336 | Common:9; Rare:69 | ||||
| chr9:132354955-132355196 | Common:3; Rare:77 | ||||
| chr9:132669974-132670039 | Common:1; Rare:33 | ||||
| chr9:133030454-133030743 | Common:4; Rare:77 | ||||
| chr9:133348039-133348258 | Common:2; Rare:86 | ||||
| chr9:133356457-133356593 | Common:1; Rare:62; Clinvar (benign):2 | ||||
| chr9:133376015-133376366 | Common:1; Rare:126 | ||||
| chr9:133417981-133418290 | Common:4; Rare:72 | ||||
| chr9:136410417-136410666 | Common:6; Rare:108 | ||||
| chr9:137188547-137188690 | Common:2; Rare:65 | ||||
| chr9:137618789-137619035 | Common:1; Rare:111 |