| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68042062-68042211 | Rare:29 | ||||
| chr11:68269997-68270133 | Common:1; Rare:22 | ||||
| chr11:68471525-68471915 | Common:1; Rare:66 | ||||
| chr11:68581705-68581955 | Common:1; Rare:37 | ||||
| chr11:68612521-68612577 | Rare:15 | ||||
| chr11:68890998-68891303 | Common:1; Rare:63 | ||||
| chr11:69011060-69011272 | Common:1; Rare:53 | ||||
| chr11:69012218-69012346 | Common:1; Rare:32 | ||||
| chr11:69321940-69322213 | Common:2; Rare:44 | ||||
| chr11:69367659-69368017 | Common:2; Rare:55 | ||||
| chr11:69642980-69643068 | Common:1; Rare:24 | ||||
| chr11:70207350-70207483 | Common:2; Rare:28 | ||||
| chr11:71994450-71994734 | Common:1; Rare:55 | ||||
| chr11:72097218-72097346 | Common:1; Rare:21 | ||||
| chr11:72234296-72234646 | Common:1; Rare:99; Clinvar (pathogenic):1 |