| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130579456-130579754 | Common:6; Rare:113 | ||||
| chr9:130693540-130693808 | Rare:86 | ||||
| chr9:130713441-130713657 | Common:2; Rare:49 | ||||
| chr9:130835095-130835459 | Common:11; Rare:114 | ||||
| chr9:131125425-131125651 | Common:2; Rare:108 | ||||
| chr9:131502853-131503046 | Rare:74; Clinvar:3 | ||||
| chr9:131531126-131531336 | Common:9; Rare:92 | ||||
| chr9:132354922-132355295 | Common:5; Rare:122 | ||||
| chr9:132669930-132670046 | Common:1; Rare:55 | ||||
| chr9:132670261-132670515 | Rare:74 | ||||
| chr9:132878272-132878411 | Common:1; Rare:53 | ||||
| chr9:133030447-133030743 | Common:4; Rare:79 | ||||
| chr9:133336116-133336314 | Common:1; Rare:87 | ||||
| chr9:133348039-133348258 | Common:2; Rare:86 | ||||
| chr9:133356443-133356630 | Common:1; Rare:87; Clinvar (benign):2 |