| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111870909-111871016 | Common:1; Rare:20 | ||||
| chr11:111871177-111871413 | Common:1; Rare:73; Clinvar:1 | ||||
| chr11:111871458-111871680 | Rare:77; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:111878306-111878679 | Common:3; Rare:77 | ||||
| chr11:111878693-111878950 | Common:2; Rare:63 | ||||
| chr11:111878974-111879102 | Common:1; Rare:60 | ||||
| chr11:111879141-111879313 | Rare:69 | ||||
| chr11:111879407-111879574 | Common:1; Rare:59 | ||||
| chr11:111879583-111879754 | Common:1; Rare:51 | ||||
| chr11:111911948-111912180 | Common:3; Rare:46 | ||||
| chr11:111918843-111918983 | Rare:34 | ||||
| chr11:111919119-111919176 | Rare:7 | ||||
| chr11:111926662-111926693 | Rare:4 | ||||
| chr11:111926811-111927356 | Common:13; Rare:110 | ||||
| chr11:111937075-111937253 | Common:5; Rare:60 |