| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:4662271-4662389 | Common:3; Rare:54 | ||||
| chr9:4679458-4679649 | Rare:93 | ||||
| chr9:5437832-5438025 | Common:1; Rare:65 | ||||
| chr9:12701087-12701391 | Rare:76 | ||||
| chr9:15510928-15511136 | Rare:79 | ||||
| chr9:19049337-19049474 | Rare:63 | ||||
| chr9:19049771-19050182 | Common:2; Rare:82 | ||||
| chr9:19102886-19103112 | Common:2; Rare:99 | ||||
| chr9:19380202-19380349 | Common:4; Rare:71 | ||||
| chr9:20684060-20684286 | Common:3; Rare:91 | ||||
| chr9:21994301-21994739 | Common:2; Rare:125; Clinvar:4; Clinvar (benign):6 | ||||
| chr9:26892417-26892532 | Rare:62 | ||||
| chr9:26892657-26892892 | Common:1; Rare:112 | ||||
| chr9:33025098-33025367 | Common:6; Rare:113 | ||||
| chr9:33076610-33076850 | Common:2; Rare:83 |