| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:24980123-24980473 | Common:10; Rare:133 | ||||
| chr7:26196557-26196875 | Common:2; Rare:130; Clinvar (benign):1 | ||||
| chr7:26200681-26201114 | Common:1; Rare:209 | ||||
| chr7:26201403-26201821 | Common:2; Rare:196 | ||||
| chr7:27096000-27096125 | Rare:36 | ||||
| chr7:27185183-27185428 | Common:1; Rare:88 | ||||
| chr7:27740067-27740202 | Common:5; Rare:34 | ||||
| chr7:30594717-30595107 | Common:6; Rare:179; Clinvar:10; Clinvar (benign):14 | ||||
| chr7:32957247-32957532 | Common:2; Rare:79 | ||||
| chr7:33062743-33062868 | Common:1; Rare:60 | ||||
| chr7:33109396-33109509 | Rare:39 | ||||
| chr7:35694888-35695251 | Common:4; Rare:102 | ||||
| chr7:35800939-35801255 | Common:2; Rare:133 | ||||
| chr7:36389539-36389881 | Common:3; Rare:106 | ||||
| chr7:40134588-40134777 | Rare:55 |