| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75914911-75915164 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994498-75994772 | Common:4; Rare:135 | ||||
| chr7:76047950-76048211 | Common:2; Rare:89 | ||||
| chr7:76302551-76303081 | Common:3; Rare:227; Clinvar:18; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76627251-76627389 | Common:5; Rare:39 | ||||
| chr7:77122036-77122183 | Common:1; Rare:28 | ||||
| chr7:77122281-77122671 | Common:2; Rare:78 | ||||
| chr7:77199393-77199430 | Rare:10 | ||||
| chr7:77199789-77199906 | Rare:28 | ||||
| chr7:77696133-77696481 | Common:1; Rare:130 | ||||
| chr7:77696515-77696960 | Common:1; Rare:190 | ||||
| chr7:77697007-77697164 | Common:1; Rare:55 | ||||
| chr7:77798379-77798971 | Common:1; Rare:141 | ||||
| chr7:79453559-79453649 | Rare:25 | ||||
| chr7:79453652-79453766 | Common:1; Rare:27 |