| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56064228-56064356 | Rare:91 | ||||
| chr7:56106363-56106381 | Rare:7 | ||||
| chr7:56106395-56106691 | Common:8; Rare:106 | ||||
| chr7:64563017-64563261 | Common:4; Rare:65 | ||||
| chr7:65006586-65006866 | Common:2; Rare:83 | ||||
| chr7:66114790-66114895 | Common:1; Rare:52 | ||||
| chr7:66115169-66115353 | Common:1; Rare:43 | ||||
| chr7:66681964-66682248 | Common:6; Rare:116 | ||||
| chr7:66921130-66921259 | Rare:41 | ||||
| chr7:66995329-66995428 | Rare:43; Clinvar (pathogenic):3 | ||||
| chr7:66996557-66996872 | Common:2; Rare:73 | ||||
| chr7:67067074-67067343 | Common:1; Rare:53 | ||||
| chr7:72828132-72828458 | Common:1; Rare:97 | ||||
| chr7:73557104-73557392 | Common:2; Rare:105 | ||||
| chr7:73557566-73557756 | Common:2; Rare:66 |