| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:22563117-22563357 | Common:1; Rare:53 | ||||
| chr7:29926641-29926943 | Common:3; Rare:65 | ||||
| chr7:32728600-32728823 | Common:7; Rare:68 | ||||
| chr7:37245213-37245498 | Common:1; Rare:62 | ||||
| chr7:40063003-40063202 | Rare:40 | ||||
| chr7:44019109-44019381 | Common:2; Rare:101 | ||||
| chr7:44038979-44039041 | Common:2; Rare:25 | ||||
| chr7:44107915-44108084 | Common:2; Rare:59; Clinvar (pathogenic):1 | ||||
| chr7:44112479-44112593 | Common:3; Rare:35 | ||||
| chr7:44113375-44113627 | Common:1; Rare:54 | ||||
| chr7:44467558-44467891 | Common:3; Rare:66 | ||||
| chr7:44581213-44581399 | Common:2; Rare:37 | ||||
| chr7:44986597-44986752 | Common:2; Rare:80 | ||||
| chr7:45768916-45769157 | Common:2; Rare:78 | ||||
| chr7:55099246-55099542 | Common:4; Rare:49 |