| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:131125446-131125630 | Common:1; Rare:84 | ||||
| chr9:132354952-132355273 | Common:5; Rare:104 | ||||
| chr9:132878277-132878410 | Common:1; Rare:49 | ||||
| chr9:133336146-133336392 | Common:2; Rare:103 | ||||
| chr9:133347977-133348237 | Common:3; Rare:83 | ||||
| chr9:133356402-133356607 | Common:1; Rare:95; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:133375973-133376366 | Common:3; Rare:143 | ||||
| chr9:133417953-133418303 | Common:4; Rare:81 | ||||
| chr9:136410446-136410678 | Common:6; Rare:107 | ||||
| chr9:136483788-136483909 | Rare:34 | ||||
| chr9:136849345-136849898 | Common:3; Rare:219 | ||||
| chr9:136944608-136944877 | Common:2; Rare:103 | ||||
| chr9:137086721-137087104 | Common:1; Rare:147; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:137113113-137113211 | Rare:48 | ||||
| chr9:137188544-137188729 | Common:2; Rare:92 |