| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14892234-14892368 | Rare:30 | ||||
| chr11:16738466-16738862 | Common:3; Rare:96 | ||||
| chr11:17013850-17013914 | Rare:17 | ||||
| chr11:17014198-17014326 | Rare:45 | ||||
| chr11:17077427-17077764 | Common:4; Rare:128 | ||||
| chr11:17207911-17208088 | Common:2; Rare:69 | ||||
| chr11:17276475-17276813 | Common:4; Rare:99; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18322130-18322312 | Common:3; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322467-18322668 | Common:2; Rare:77 | ||||
| chr11:18526841-18526982 | Rare:70 | ||||
| chr11:18588671-18588929 | Common:3; Rare:84 | ||||
| chr11:18634317-18634498 | Common:1; Rare:62 | ||||
| chr11:18698505-18698747 | Common:3; Rare:54 | ||||
| chr11:18791736-18791912 | Rare:57 | ||||
| chr11:19713512-19713725 | Rare:57 |