| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:25831781-25831940 | Common:1; Rare:30 | ||||
| chr7:25951324-25951539 | Common:2; Rare:58 | ||||
| chr7:26130733-26131120 | Common:2; Rare:75 | ||||
| chr7:26193252-26193696 | Rare:156; Clinvar (benign):2 | ||||
| chr7:26244906-26245104 | Rare:48 | ||||
| chr7:26376062-26376220 | Common:2; Rare:50 | ||||
| chr7:26376690-26376763 | Rare:16 | ||||
| chr7:26398827-26398969 | Common:2; Rare:38 | ||||
| chr7:26399397-26399448 | Common:1; Rare:9 | ||||
| chr7:26637763-26637934 | Rare:22 | ||||
| chr7:26638241-26638358 | Common:3; Rare:27 | ||||
| chr7:26805142-26805267 | Common:1; Rare:32 | ||||
| chr7:27088048-27088221 | Common:2; Rare:38 | ||||
| chr7:27380095-27380273 | Rare:24 | ||||
| chr7:27387175-27387309 | Common:2; Rare:21 |