| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:66995289-66995326 | Common:1; Rare:12; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr7:66996554-66996924 | Common:2; Rare:89 | ||||
| chr7:72828133-72828472 | Common:1; Rare:98 | ||||
| chr7:73308722-73308877 | Rare:68 | ||||
| chr7:73522211-73522438 | Common:2; Rare:71 | ||||
| chr7:73557491-73557783 | Common:2; Rare:96 | ||||
| chr7:73683386-73683670 | Common:4; Rare:131 | ||||
| chr7:73686684-73686872 | Common:3; Rare:51 | ||||
| chr7:74174080-74174429 | Common:1; Rare:163 | ||||
| chr7:74209763-74210050 | Common:1; Rare:68 | ||||
| chr7:74254327-74254535 | Rare:96 | ||||
| chr7:74289287-74289461 | Common:3; Rare:68 | ||||
| chr7:75882200-75882482 | Common:2; Rare:75 | ||||
| chr7:75914941-75915191 | Common:2; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:75994475-75994781 | Common:4; Rare:147 |