| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:33129491-33129586 | Rare:24 | ||||
| chr7:39566312-39566435 | Common:1; Rare:59 | ||||
| chr7:39623514-39623808 | Rare:93 | ||||
| chr7:40134562-40134802 | Rare:72 | ||||
| chr7:40134843-40135009 | Rare:59 | ||||
| chr7:41700569-41700663 | Rare:14 | ||||
| chr7:42932160-42932384 | Rare:84 | ||||
| chr7:43926398-43926457 | Rare:23 | ||||
| chr7:44490573-44490956 | Common:1; Rare:129 | ||||
| chr7:44573854-44574045 | Common:3; Rare:65 | ||||
| chr7:47582050-47582334 | Common:1; Rare:80 | ||||
| chr7:48089073-48089285 | Common:2; Rare:58 | ||||
| chr7:50450336-50450441 | Rare:42 | ||||
| chr7:56051405-56051857 | Common:1; Rare:172; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:66114732-66114851 | Common:1; Rare:51 |