| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74174125-74174386 | Common:1; Rare:138 | ||||
| chr7:74209836-74210021 | Rare:48 | ||||
| chr7:74254366-74254528 | Rare:75 | ||||
| chr7:75914898-75915168 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994614-75994772 | Common:3; Rare:80 | ||||
| chr7:76047954-76048188 | Common:2; Rare:78 | ||||
| chr7:76302852-76303073 | Rare:92; Clinvar:10; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:77122357-77122672 | Common:1; Rare:66 | ||||
| chr7:77696133-77696475 | Common:1; Rare:127 | ||||
| chr7:77798449-77798916 | Common:1; Rare:121 | ||||
| chr7:79453580-79453634 | Rare:18 | ||||
| chr7:79453659-79454117 | Common:3; Rare:109 | ||||
| chr7:80918939-80919287 | Common:3; Rare:106 | ||||
| chr7:87152102-87152474 | Common:3; Rare:106 | ||||
| chr7:87345451-87345701 | Common:4; Rare:84 |