| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:4642086-4642345 | Common:9; Rare:191 | ||||
| chr7:4973986-4974149 | Common:1; Rare:76 | ||||
| chr7:5397172-5397451 | Rare:145 | ||||
| chr7:5419088-5419288 | Rare:62 | ||||
| chr7:5427938-5428338 | Common:3; Rare:232 | ||||
| chr7:5531376-5531620 | Common:2; Rare:118 | ||||
| chr7:5555080-5555320 | Common:2; Rare:115 | ||||
| chr7:5555750-5556120 | Common:4; Rare:137 | ||||
| chr7:5556551-5556776 | Common:1; Rare:66 | ||||
| chr7:5570160-5570331 | Common:4; Rare:106 | ||||
| chr7:5823007-5823284 | Common:9; Rare:205 | ||||
| chr7:5995570-5995870 | Common:2; Rare:124; Clinvar:23; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr7:6080830-6081270 | Common:4; Rare:187 | ||||
| chr7:6081402-6081730 | Common:4; Rare:216 | ||||
| chr7:6367881-6368281 | Rare:204 |