| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:129835137-129835499 | Common:4; Rare:142 | ||||
| chr9:129879223-129879422 | Common:2; Rare:40 | ||||
| chr9:130043090-130043291 | Common:2; Rare:62 | ||||
| chr9:130053847-130054031 | Common:1; Rare:69 | ||||
| chr9:130444726-130444991 | Common:1; Rare:76; Clinvar:8; Clinvar (benign):1 | ||||
| chr9:130451929-130452303 | Common:2; Rare:105; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr9:130579428-130579692 | Common:7; Rare:106 | ||||
| chr9:130693602-130693813 | Rare:77 | ||||
| chr9:131125446-131125657 | Common:1; Rare:101 | ||||
| chr9:131502860-131503016 | Rare:57; Clinvar:3 | ||||
| chr9:131531175-131531359 | Common:9; Rare:85 | ||||
| chr9:132354915-132355283 | Common:5; Rare:119 | ||||
| chr9:132669930-132670048 | Common:1; Rare:55 | ||||
| chr9:132878272-132878374 | Common:1; Rare:36 | ||||
| chr9:133030447-133030761 | Common:4; Rare:89 |