| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66531457-66531740 | Rare:65; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:66622895-66623227 | Common:1; Rare:66 | ||||
| chr11:66841047-66841160 | Common:2; Rare:19 | ||||
| chr11:67332843-67333031 | Rare:27 | ||||
| chr11:67438902-67439041 | Rare:49 | ||||
| chr11:67441130-67441353 | Common:1; Rare:82 | ||||
| chr11:68040410-68040539 | Rare:30 | ||||
| chr11:68054078-68054349 | Rare:77 | ||||
| chr11:68056352-68056556 | Common:2; Rare:40 | ||||
| chr11:68107852-68108010 | Common:1; Rare:30 | ||||
| chr11:68762736-68762883 | Common:2; Rare:35 | ||||
| chr11:69985543-69985818 | Common:5; Rare:67 | ||||
| chr11:72004224-72004439 | Rare:72 | ||||
| chr11:72005262-72005538 | Common:1; Rare:62 | ||||
| chr11:72018228-72018353 | Common:2; Rare:32 |