| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151083262-151083569 | Common:3; Rare:64 | ||||
| chr7:151085682-151085919 | Common:1; Rare:44 | ||||
| chr7:151227153-151227514 | Common:2; Rare:91 | ||||
| chr7:151232382-151232528 | Common:1; Rare:48 | ||||
| chr7:151277119-151277214 | Rare:30 | ||||
| chr7:151341555-151341864 | Common:4; Rare:96 | ||||
| chr7:151410028-151410164 | Rare:42 | ||||
| chr7:151736456-151736621 | Rare:26 | ||||
| chr7:152025567-152025807 | Rare:94 | ||||
| chr7:152435916-152436269 | Rare:119 | ||||
| chr7:152676091-152676310 | Common:2; Rare:99; Clinvar (benign):10 | ||||
| chr7:152759644-152759825 | Common:4; Rare:74 | ||||
| chr7:155002933-155003147 | Common:3; Rare:65 | ||||
| chr7:155003277-155003518 | Common:6; Rare:98 | ||||
| chr7:155644320-155644734 | Common:2; Rare:137 |