| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:25125060-25125608 | Common:2; Rare:195; Clinvar:3 | ||||
| chr7:25180299-25180503 | Common:1; Rare:71 | ||||
| chr7:26200572-26201271 | Common:3; Rare:323 | ||||
| chr7:26201362-26201856 | Common:2; Rare:226 | ||||
| chr7:26202078-26202426 | Rare:154 | ||||
| chr7:26864588-26864806 | Common:2; Rare:70 | ||||
| chr7:27662795-27663148 | Common:6; Rare:126 | ||||
| chr7:27740022-27740212 | Common:5; Rare:61 | ||||
| chr7:28180539-28180861 | Common:4; Rare:88 | ||||
| chr7:29193809-29194010 | Common:1; Rare:28 | ||||
| chr7:29194074-29194630 | Rare:145 | ||||
| chr7:29194662-29194987 | Common:2; Rare:87 | ||||
| chr7:30026399-30026794 | Rare:115; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr7:30028314-30028663 | Common:2; Rare:112 | ||||
| chr7:30135029-30135256 | Common:3; Rare:74 |