| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67421102-67421411 | Common:4; Rare:104 | ||||
| chr11:67428090-67428586 | Common:1; Rare:152 | ||||
| chr11:67428918-67428977 | Rare:13 | ||||
| chr11:67429261-67429314 | Rare:14 | ||||
| chr11:67442856-67442975 | Common:1; Rare:24 | ||||
| chr11:67443405-67443647 | Common:3; Rare:87 | ||||
| chr11:67443662-67443817 | Rare:38 | ||||
| chr11:67464609-67464972 | Rare:178 | ||||
| chr11:67465256-67465521 | Rare:53 | ||||
| chr11:67468195-67468374 | Common:3; Rare:26 | ||||
| chr11:67468784-67468954 | Common:1; Rare:50 | ||||
| chr11:67469116-67469478 | Common:4; Rare:125 | ||||
| chr11:67482825-67483218 | Common:1; Rare:98; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr11:67483243-67483501 | Rare:83; Clinvar (benign):1 | ||||
| chr11:67505294-67505476 | Rare:44 |