| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:56051371-56051857 | Common:1; Rare:179; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56051960-56051985 | Rare:4 | ||||
| chr7:56064186-56064347 | Common:2; Rare:102 | ||||
| chr7:64563024-64563261 | Common:4; Rare:64 | ||||
| chr7:64665979-64666206 | Common:4; Rare:50 | ||||
| chr7:64794248-64794471 | Common:4; Rare:67 | ||||
| chr7:65982174-65982416 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:66114799-66114952 | Common:1; Rare:66 | ||||
| chr7:66115188-66115354 | Rare:38 | ||||
| chr7:72828136-72828444 | Common:1; Rare:91 | ||||
| chr7:73683410-73683638 | Common:3; Rare:98 | ||||
| chr7:73738786-73739146 | Common:2; Rare:114 | ||||
| chr7:74174114-74174441 | Common:1; Rare:158 | ||||
| chr7:74254304-74254692 | Rare:142 | ||||
| chr7:74657380-74657738 | Common:2; Rare:110 |