| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151232382-151232533 | Common:1; Rare:53 | ||||
| chr7:151277130-151277248 | Rare:34 | ||||
| chr7:151341578-151341897 | Common:5; Rare:96 | ||||
| chr7:151736228-151736621 | Common:6; Rare:75 | ||||
| chr7:151877165-151877525 | Common:2; Rare:102; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:152025549-152025802 | Common:1; Rare:101 | ||||
| chr7:152435916-152436291 | Rare:128 | ||||
| chr7:152676073-152676301 | Common:2; Rare:98; Clinvar (benign):12 | ||||
| chr7:152759633-152759851 | Common:4; Rare:85 | ||||
| chr7:155644372-155644724 | Common:2; Rare:121 | ||||
| chr7:155645196-155645269 | Common:2; Rare:24 | ||||
| chr7:156640535-156640794 | Common:3; Rare:122 | ||||
| chr7:156949488-156949794 | Common:3; Rare:103 | ||||
| chr7:156949921-156950115 | Common:5; Rare:68 | ||||
| chr7:157010626-157010926 | Common:5; Rare:93 |