| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128275919-128276327 | Common:5; Rare:187 | ||||
| chr9:128322410-128322485 | Rare:30 | ||||
| chr9:128322760-128322880 | Common:2; Rare:61; Clinvar (benign):5 | ||||
| chr9:128371225-128371425 | Rare:78 | ||||
| chr9:128504605-128504785 | Rare:83; Clinvar:5 | ||||
| chr9:128552408-128552611 | Rare:79; Clinvar:1 | ||||
| chr9:128656635-128656794 | Common:2; Rare:75; Clinvar (pathogenic):1 | ||||
| chr9:128724095-128724464 | Common:2; Rare:121 | ||||
| chr9:128771871-128772135 | Common:4; Rare:70 | ||||
| chr9:128881907-128882192 | Common:1; Rare:94 | ||||
| chr9:128921964-128922320 | Common:1; Rare:77 | ||||
| chr9:128947598-128947725 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129110671-129110953 | Common:3; Rare:64 | ||||
| chr9:129111219-129111456 | Common:2; Rare:83 | ||||
| chr9:129141884-129142041 | Common:3; Rare:35 |