| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151028119-151028493 | Rare:132 | ||||
| chr7:151028656-151028753 | Rare:24 | ||||
| chr7:151057884-151058205 | Common:3; Rare:82 | ||||
| chr7:151059445-151059621 | Common:1; Rare:54 | ||||
| chr7:151082929-151083192 | Rare:46 | ||||
| chr7:151083514-151083823 | Rare:65 | ||||
| chr7:151227166-151227405 | Common:1; Rare:66 | ||||
| chr7:151876666-151876758 | Common:1; Rare:16; Clinvar (benign):1 | ||||
| chr7:152676132-152676323 | Common:2; Rare:83 | ||||
| chr7:155003361-155003462 | Common:2; Rare:49 | ||||
| chr7:155297537-155297860 | Common:5; Rare:120 | ||||
| chr7:155298833-155299145 | Common:2; Rare:57 | ||||
| chr7:155644384-155644719 | Common:2; Rare:112 | ||||
| chr7:157336880-157337013 | Rare:53 | ||||
| chr8:406749-407033 | Common:4; Rare:132 |