| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127899518-127899752 | Common:1; Rare:84 | ||||
| chr9:127937816-127937923 | Common:1; Rare:31; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:128091285-128091492 | Rare:42 | ||||
| chr9:128160046-128160391 | Common:2; Rare:85 | ||||
| chr9:128275936-128276307 | Common:5; Rare:171 | ||||
| chr9:128322376-128322659 | Common:1; Rare:93 | ||||
| chr9:128322713-128322866 | Common:2; Rare:57; Clinvar (benign):5 | ||||
| chr9:128371196-128371426 | Rare:89 | ||||
| chr9:128455948-128456192 | Common:1; Rare:78 | ||||
| chr9:128504605-128504793 | Rare:87; Clinvar:5 | ||||
| chr9:128552394-128552612 | Rare:81; Clinvar:1 | ||||
| chr9:128656646-128656816 | Common:2; Rare:75; Clinvar (pathogenic):1 | ||||
| chr9:128689534-128689653 | Rare:48 | ||||
| chr9:128724070-128724480 | Common:4; Rare:137 | ||||
| chr9:128771885-128772048 | Common:1; Rare:42 |