| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:64794245-64794476 | Common:8; Rare:123 | ||||
| chr7:65006577-65006876 | Common:5; Rare:150 | ||||
| chr7:65982164-65982353 | Common:6; Rare:122; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr7:66075570-66075980 | Rare:108; Clinvar (benign):1 | ||||
| chr7:66114727-66114937 | Common:3; Rare:159 | ||||
| chr7:66115166-66115380 | Common:1; Rare:93 | ||||
| chr7:66150321-66150742 | Common:1; Rare:105 | ||||
| chr7:66205037-66205395 | Common:2; Rare:123 | ||||
| chr7:66628632-66629000 | Common:4; Rare:268; Clinvar:11 | ||||
| chr7:66682000-66682241 | Common:11; Rare:195 | ||||
| chr7:66921088-66921377 | Common:1; Rare:155 | ||||
| chr7:66995449-66995647 | Rare:55 | ||||
| chr7:66996554-66996929 | Common:4; Rare:175 | ||||
| chr7:72828124-72828504 | Common:1; Rare:179 | ||||
| chr7:72924990-72925190 | Common:5; Rare:100 |