| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:15073431-15073598 | Common:2; Rare:33 | ||||
| chr11:16738432-16738729 | Common:3; Rare:68 | ||||
| chr11:17014255-17014321 | Rare:23 | ||||
| chr11:17077427-17077974 | Common:4; Rare:218 | ||||
| chr11:17207920-17208174 | Common:1; Rare:99 | ||||
| chr11:17276532-17276828 | Common:5; Rare:85; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:17351618-17351827 | Common:1; Rare:44 | ||||
| chr11:17351870-17352320 | Common:3; Rare:90 | ||||
| chr11:17389325-17389460 | Common:1; Rare:28 | ||||
| chr11:17476748-17476968 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:17547080-17547290 | Rare:41 | ||||
| chr11:18012875-18013248 | Common:6; Rare:126 | ||||
| chr11:18105989-18106207 | Common:2; Rare:92 | ||||
| chr11:18322077-18322330 | Common:4; Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322447-18322629 | Common:2; Rare:70 |