| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:45917505-45917827 | Common:5; Rare:65 | ||||
| chr7:45920144-45920473 | Common:3; Rare:68 | ||||
| chr7:45921269-45921374 | Rare:27 | ||||
| chr7:47481254-47481437 | Rare:31 | ||||
| chr7:47582043-47582198 | Common:1; Rare:46 | ||||
| chr7:47582504-47582732 | Rare:57 | ||||
| chr7:47979500-47979747 | Rare:90 | ||||
| chr7:48088871-48089278 | Common:6; Rare:104 | ||||
| chr7:50450322-50450453 | Common:1; Rare:54 | ||||
| chr7:55365935-55366082 | Rare:62 | ||||
| chr7:56051405-56051878 | Common:1; Rare:178; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064145-56064367 | Common:2; Rare:131 | ||||
| chr7:56106389-56106711 | Common:9; Rare:112 | ||||
| chr7:66114773-66114904 | Common:1; Rare:65 | ||||
| chr7:66115177-66115374 | Common:1; Rare:45 |