| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:125111149-125111338 | Rare:33 | ||||
| chr11:125111707-125112060 | Common:3; Rare:74 | ||||
| chr11:125569210-125569493 | Common:1; Rare:78 | ||||
| chr11:125591567-125591794 | Common:1; Rare:48 | ||||
| chr11:125592433-125592937 | Common:6; Rare:174; Clinvar (benign):1 | ||||
| chr11:125593436-125593565 | Rare:30 | ||||
| chr11:125625489-125626032 | Common:4; Rare:174 | ||||
| chr11:125626211-125626278 | Rare:19 | ||||
| chr11:125887076-125887167 | Rare:26 | ||||
| chr11:125887187-125887275 | Rare:21 | ||||
| chr11:125887451-125887819 | Common:2; Rare:109 | ||||
| chr11:125887926-125888241 | Common:2; Rare:90 | ||||
| chr11:125903099-125903252 | Common:1; Rare:31 | ||||
| chr11:126211232-126211431 | Rare:44 | ||||
| chr11:126211593-126211858 | Rare:121 |