| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128340419-128340748 | Common:2; Rare:100 | ||||
| chr9:128371120-128371404 | Common:1; Rare:94 | ||||
| chr9:128504601-128504828 | Rare:105; Clinvar:6 | ||||
| chr9:128552394-128552602 | Rare:76; Clinvar:1 | ||||
| chr9:128656640-128657002 | Common:2; Rare:120; Clinvar (pathogenic):1 | ||||
| chr9:128683250-128683487 | Common:6; Rare:31 | ||||
| chr9:128683642-128683912 | Rare:70 | ||||
| chr9:128724072-128724467 | Common:2; Rare:133 | ||||
| chr9:128771833-128771980 | Rare:42 | ||||
| chr9:128881896-128882186 | Common:1; Rare:94 | ||||
| chr9:128921964-128922324 | Common:1; Rare:79 | ||||
| chr9:128947549-128947738 | Common:1; Rare:90; Clinvar:6; Clinvar (benign):1 | ||||
| chr9:129110570-129110950 | Common:3; Rare:82 | ||||
| chr9:129642107-129642455 | Common:4; Rare:88 | ||||
| chr9:129824070-129824299 | Common:3; Rare:64; Clinvar:2; Clinvar (benign):2 |