| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128552398-128552611 | Rare:81; Clinvar:1 | ||||
| chr9:128684939-128685075 | Rare:23 | ||||
| chr9:128724095-128724464 | Common:2; Rare:121 | ||||
| chr9:128787143-128787341 | Common:3; Rare:68 | ||||
| chr9:128881915-128882192 | Common:1; Rare:92 | ||||
| chr9:128947593-128947722 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129110671-129110950 | Common:3; Rare:62 | ||||
| chr9:129752955-129753165 | Common:2; Rare:67 | ||||
| chr9:129835210-129835475 | Common:2; Rare:108 | ||||
| chr9:130053860-130053960 | Common:1; Rare:39 | ||||
| chr9:130693594-130693794 | Rare:64 | ||||
| chr9:131125402-131125661 | Common:2; Rare:122 | ||||
| chr9:131531175-131531344 | Common:9; Rare:77 | ||||
| chr9:132669936-132670046 | Common:1; Rare:53 | ||||
| chr9:132878279-132878385 | Common:1; Rare:38 |