| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75878847-75879076 | Common:12; Rare:83 | ||||
| chr7:75914914-75915164 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:76047939-76048179 | Common:1; Rare:82 | ||||
| chr7:77696219-77696460 | Rare:92 | ||||
| chr7:77798576-77798888 | Common:1; Rare:94 | ||||
| chr7:87152319-87152468 | Common:1; Rare:47 | ||||
| chr7:87345477-87345701 | Common:4; Rare:71 | ||||
| chr7:87876324-87876653 | Common:2; Rare:142 | ||||
| chr7:90346616-90346744 | Common:3; Rare:62 | ||||
| chr7:91880677-91880823 | Common:2; Rare:39 | ||||
| chr7:91940732-91940872 | Common:2; Rare:36 | ||||
| chr7:91940875-91940958 | Common:2; Rare:28; Clinvar:2 | ||||
| chr7:92528392-92528816 | Common:3; Rare:135; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93890710-93890947 | Common:3; Rare:57 | ||||
| chr7:94656114-94656379 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2 |