| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33736375-33736566 | Common:2; Rare:65 | ||||
| chr11:34051605-34051736 | Rare:54 | ||||
| chr11:34052002-34052624 | Common:5; Rare:268 | ||||
| chr11:34105478-34105764 | Common:2; Rare:93 | ||||
| chr11:34620848-34621166 | Common:2; Rare:67 | ||||
| chr11:34916300-34916687 | Common:10; Rare:159; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139391 | Common:1; Rare:123 | ||||
| chr11:35201423-35201788 | Common:2; Rare:78 | ||||
| chr11:35218986-35219288 | Common:3; Rare:62 | ||||
| chr11:35619108-35619314 | Rare:69 | ||||
| chr11:35943923-35944143 | Common:4; Rare:70 | ||||
| chr11:36289370-36289441 | Rare:35 | ||||
| chr11:36510240-36510365 | Rare:35 | ||||
| chr11:43358813-43359001 | Rare:92 | ||||
| chr11:46120952-46121252 | Common:2; Rare:44 |