| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:90595843-90596028 | Common:6; Rare:62 | ||||
| chr7:90596312-90596469 | Rare:53 | ||||
| chr7:91880668-91880768 | Common:1; Rare:29 | ||||
| chr7:91940755-91941004 | Common:4; Rare:80; Clinvar:4; Clinvar (benign):1 | ||||
| chr7:92105628-92105745 | Rare:35; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:92134364-92134568 | Rare:62 | ||||
| chr7:92134717-92134884 | Common:3; Rare:51 | ||||
| chr7:92245655-92246451 | Common:6; Rare:230; Clinvar:4; Clinvar (benign):5 | ||||
| chr7:92447224-92447516 | Common:3; Rare:88 | ||||
| chr7:92528306-92528816 | Common:3; Rare:152; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr7:93226414-93226783 | Common:5; Rare:57 | ||||
| chr7:93232194-93232412 | Common:2; Rare:45 | ||||
| chr7:94004283-94004472 | Rare:51 | ||||
| chr7:94394775-94394923 | Rare:30 | ||||
| chr7:94509447-94509677 | Common:3; Rare:57 |