| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:27180134-27180438 | Common:4; Rare:83 | ||||
| chr7:27185180-27185433 | Common:1; Rare:90 | ||||
| chr7:27662762-27663171 | Common:7; Rare:141 | ||||
| chr7:27740067-27740206 | Common:5; Rare:35 | ||||
| chr7:28958258-28958616 | Rare:95 | ||||
| chr7:28958635-28958670 | Rare:10 | ||||
| chr7:29563687-29563855 | Rare:44 | ||||
| chr7:30504747-30505081 | Common:2; Rare:110 | ||||
| chr7:30594709-30594909 | Common:3; Rare:84; Clinvar:5; Clinvar (benign):5 | ||||
| chr7:30771286-30771488 | Common:1; Rare:67 | ||||
| chr7:32495231-32495602 | Common:1; Rare:97 | ||||
| chr7:33129227-33129592 | Common:5; Rare:102 | ||||
| chr7:33905354-33905586 | Common:2; Rare:42; Clinvar:1 | ||||
| chr7:35695133-35695260 | Common:1; Rare:43 | ||||
| chr7:35800721-35801264 | Common:2; Rare:207 |