| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128947580-128947725 | Common:1; Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129110625-129110949 | Common:3; Rare:72 | ||||
| chr9:129835228-129835486 | Common:2; Rare:102 | ||||
| chr9:130053847-130053933 | Common:1; Rare:26 | ||||
| chr9:131125407-131125637 | Common:2; Rare:105 | ||||
| chr9:132669939-132670051 | Common:1; Rare:53 | ||||
| chr9:133336128-133336335 | Common:1; Rare:83 | ||||
| chr9:133348034-133348276 | Common:3; Rare:100 | ||||
| chr9:133356476-133356607 | Common:1; Rare:60; Clinvar (benign):2 | ||||
| chr9:133376015-133376332 | Common:1; Rare:114 | ||||
| chr9:133524890-133525127 | Common:2; Rare:39 | ||||
| chr9:136410582-136410671 | Common:1; Rare:49 | ||||
| chr9:136662787-136662927 | Common:1; Rare:39 | ||||
| chr9:136849591-136849772 | Common:1; Rare:69 | ||||
| chr9:137188547-137188717 | Common:2; Rare:85 |