| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:74254357-74254535 | Rare:84 | ||||
| chr7:76047950-76048188 | Common:2; Rare:81 | ||||
| chr7:76302481-76302700 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:76302890-76303009 | Rare:50; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:77537942-77538078 | Common:4; Rare:57 | ||||
| chr7:77696214-77696465 | Rare:99 | ||||
| chr7:77798387-77798859 | Common:1; Rare:112 | ||||
| chr7:79453560-79454109 | Common:3; Rare:135 | ||||
| chr7:80919035-80919347 | Common:3; Rare:112 | ||||
| chr7:87152301-87152474 | Common:1; Rare:56 | ||||
| chr7:87345461-87345722 | Common:5; Rare:85 | ||||
| chr7:87876224-87876643 | Common:2; Rare:179 | ||||
| chr7:90211633-90211886 | Common:3; Rare:77 | ||||
| chr7:90346596-90346736 | Common:3; Rare:59 | ||||
| chr7:91880677-91880801 | Common:1; Rare:33 |