| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43172270-43172454 | Common:1; Rare:34 | ||||
| chr6:44253878-44254147 | Common:1; Rare:87 | ||||
| chr6:57961375-57961558 | Common:1; Rare:56 | ||||
| chr6:169162801-169163271 | Common:3; Rare:99 | ||||
| chr7:29684924-29684991 | Rare:24 | ||||
| chr7:32727876-32728146 | Common:2; Rare:83 | ||||
| chr7:32754850-32755120 | Common:1; Rare:57 | ||||
| chr7:32942468-32942696 | Common:2; Rare:64 | ||||
| chr7:38335583-38335808 | Common:2; Rare:51 | ||||
| chr7:41705407-41705646 | Common:1; Rare:54 | ||||
| chr7:44019134-44019390 | Common:2; Rare:86 | ||||
| chr7:44107902-44108083 | Common:2; Rare:65; Clinvar (pathogenic):1 | ||||
| chr7:65750913-65751078 | Common:2; Rare:67 | ||||
| chr7:66493560-66493740 | Common:3; Rare:69 | ||||
| chr7:66654456-66654567 | Rare:39 |