| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127579254-127579287 | Rare:9 | ||||
| chr9:127612040-127612344 | Common:1; Rare:114; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:127802737-127803032 | Common:3; Rare:81 | ||||
| chr9:127803148-127803306 | Common:1; Rare:36 | ||||
| chr9:127877662-127877786 | Rare:24 | ||||
| chr9:127916972-127917281 | Common:1; Rare:91 | ||||
| chr9:128098291-128098549 | Common:1; Rare:55 | ||||
| chr9:128128404-128128517 | Common:2; Rare:56 | ||||
| chr9:128160040-128160459 | Common:2; Rare:103 | ||||
| chr9:128190415-128190721 | Rare:82 | ||||
| chr9:128191479-128191642 | Rare:50 | ||||
| chr9:128191750-128191857 | Common:1; Rare:26 | ||||
| chr9:128275919-128276327 | Common:5; Rare:187 | ||||
| chr9:128322410-128322649 | Common:1; Rare:67 | ||||
| chr9:128322718-128322894 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 |