| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:130579428-130579671 | Common:4; Rare:91 | ||||
| chr9:130693565-130693800 | Rare:77 | ||||
| chr9:131125425-131125657 | Common:2; Rare:110 | ||||
| chr9:131531188-131531351 | Common:9; Rare:73 | ||||
| chr9:132354936-132355208 | Common:3; Rare:85 | ||||
| chr9:132669939-132670040 | Common:1; Rare:49 | ||||
| chr9:132878314-132878370 | Common:1; Rare:17 | ||||
| chr9:133030442-133030743 | Common:4; Rare:83 | ||||
| chr9:133336141-133336345 | Common:1; Rare:79 | ||||
| chr9:133348039-133348276 | Common:2; Rare:99 | ||||
| chr9:133356470-133356593 | Common:1; Rare:53; Clinvar (benign):2 | ||||
| chr9:133376010-133376330 | Common:1; Rare:116 | ||||
| chr9:133418044-133418296 | Common:3; Rare:50 | ||||
| chr9:133479061-133479392 | Common:1; Rare:97 | ||||
| chr9:133703531-133703790 | Common:3; Rare:56 |