| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:23105673-23105819 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:23181860-23182135 | Common:2; Rare:115 | ||||
| chr7:23679921-23680233 | Common:5; Rare:94 | ||||
| chr7:24757395-24757640 | Common:2; Rare:72 | ||||
| chr7:24980100-24980357 | Common:6; Rare:105 | ||||
| chr7:25125205-25125444 | Rare:106; Clinvar:3 | ||||
| chr7:26200593-26201008 | Common:2; Rare:200 | ||||
| chr7:26201414-26201442 | Rare:10 | ||||
| chr7:26201568-26201800 | Common:2; Rare:125 | ||||
| chr7:27095976-27096205 | Rare:67 | ||||
| chr7:27140197-27140483 | Common:1; Rare:64 | ||||
| chr7:27165172-27165247 | Rare:31 | ||||
| chr7:27740047-27740209 | Common:5; Rare:46 | ||||
| chr7:28180597-28180888 | Common:4; Rare:74 | ||||
| chr7:29194631-29194902 | Common:1; Rare:66 |