| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75486249-75486506 | Common:2; Rare:91 | ||||
| chr7:75562962-75563199 | Rare:76 | ||||
| chr7:75878859-75879083 | Common:12; Rare:85 | ||||
| chr7:75914898-75915176 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:75994538-75994779 | Common:4; Rare:130 | ||||
| chr7:76047893-76048206 | Common:3; Rare:108 | ||||
| chr7:76302867-76303054 | Rare:83; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr7:76303614-76303817 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:77536880-77537043 | Common:2; Rare:51 | ||||
| chr7:77696229-77696475 | Rare:99 | ||||
| chr7:77798353-77798949 | Common:1; Rare:144 | ||||
| chr7:87152275-87152474 | Common:1; Rare:69 | ||||
| chr7:87220526-87220682 | Common:1; Rare:45 | ||||
| chr7:87345469-87345701 | Common:4; Rare:76 | ||||
| chr7:87876250-87876735 | Common:3; Rare:209 |