| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128191505-128191885 | Common:2; Rare:96 | ||||
| chr9:128275914-128276293 | Common:4; Rare:167 | ||||
| chr9:128371196-128371398 | Rare:75 | ||||
| chr9:128552408-128552604 | Rare:75; Clinvar:1 | ||||
| chr9:128683529-128683844 | Rare:60 | ||||
| chr9:128724068-128724283 | Common:1; Rare:77 | ||||
| chr9:128881929-128882205 | Common:2; Rare:94 | ||||
| chr9:128947537-128947719 | Common:1; Rare:81; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:129141906-129142039 | Common:3; Rare:27 | ||||
| chr9:129803047-129803164 | Common:2; Rare:30 | ||||
| chr9:129835210-129835458 | Common:2; Rare:104 | ||||
| chr9:130579431-130579662 | Common:4; Rare:80 | ||||
| chr9:133348039-133348260 | Common:2; Rare:88 | ||||
| chr9:133356408-133356580 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:133375979-133376366 | Common:3; Rare:140 |