| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:88220003-88220182 | Rare:80 | ||||
| chr7:90211628-90211775 | Common:2; Rare:41 | ||||
| chr7:90346586-90346733 | Common:3; Rare:62 | ||||
| chr7:91880677-91880820 | Common:1; Rare:38 | ||||
| chr7:92134427-92134890 | Common:5; Rare:134 | ||||
| chr7:92245857-92245974 | Rare:33; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:92528434-92528807 | Common:3; Rare:116; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:93117934-93118123 | Rare:30 | ||||
| chr7:93232201-93232385 | Common:2; Rare:33 | ||||
| chr7:94656122-94656367 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr7:95434895-95435079 | Common:1; Rare:83; Clinvar (benign):1 | ||||
| chr7:98252131-98252364 | Common:1; Rare:52 | ||||
| chr7:98282045-98282383 | Common:2; Rare:110 | ||||
| chr7:99325766-99325987 | Common:1; Rare:90 | ||||
| chr7:99408545-99409081 | Common:3; Rare:152 |