| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151059486-151059709 | Common:1; Rare:67 | ||||
| chr7:151075497-151075636 | Rare:40 | ||||
| chr7:151080749-151080962 | Rare:67 | ||||
| chr7:151227158-151227436 | Common:1; Rare:75 | ||||
| chr7:151232382-151232532 | Common:1; Rare:52 | ||||
| chr7:151249108-151249325 | Common:2; Rare:50 | ||||
| chr7:151877149-151877531 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:152025564-152025791 | Rare:91 | ||||
| chr7:152676128-152676268 | Common:2; Rare:48 | ||||
| chr7:152759639-152759825 | Common:4; Rare:75 | ||||
| chr7:155644357-155644730 | Common:2; Rare:130 | ||||
| chr7:155812126-155812237 | Common:2; Rare:21 | ||||
| chr7:156640535-156640806 | Common:4; Rare:124 | ||||
| chr7:156893154-156893414 | Common:4; Rare:104; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:157336770-157336792 | Rare:14 |