| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:25125220-25125670 | Rare:179; Clinvar:3 | ||||
| chr7:26152634-26153064 | Common:1; Rare:138 | ||||
| chr7:26183646-26183713 | Common:1; Rare:39 | ||||
| chr7:26196555-26197268 | Common:5; Rare:270; Clinvar (benign):3 | ||||
| chr7:26200166-26200425 | Common:3; Rare:130 | ||||
| chr7:26200567-26201148 | Common:2; Rare:269 | ||||
| chr7:26201392-26201555 | Rare:60 | ||||
| chr7:26201558-26201839 | Common:2; Rare:141 | ||||
| chr7:26202078-26202397 | Rare:140 | ||||
| chr7:26202589-26202890 | Common:1; Rare:102 | ||||
| chr7:26864365-26864421 | Common:1; Rare:17 | ||||
| chr7:27095917-27096238 | Rare:88 | ||||
| chr7:27102109-27102302 | Rare:61 | ||||
| chr7:27102662-27102829 | Rare:33; Clinvar:2 | ||||
| chr7:27113377-27113587 | Rare:39 |