| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:108497947-108498134 | Common:1; Rare:42 | ||||
| chr11:108593760-108593916 | Common:4; Rare:43 | ||||
| chr11:110296470-110296797 | Common:2; Rare:148; Clinvar:9 | ||||
| chr11:111299656-111299769 | Common:2; Rare:29 | ||||
| chr11:111540476-111540757 | Common:1; Rare:68 | ||||
| chr11:111541539-111541558 | Common:1; Rare:2 | ||||
| chr11:111602311-111602584 | Common:1; Rare:92 | ||||
| chr11:111766338-111766426 | Rare:48 | ||||
| chr11:111871254-111871379 | Rare:40; Clinvar:1 | ||||
| chr11:111871498-111871629 | Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:111878655-111878961 | Common:2; Rare:82 | ||||
| chr11:111879147-111879583 | Common:1; Rare:142 | ||||
| chr11:111912134-111912230 | Rare:12 | ||||
| chr11:111912720-111912842 | Rare:20 | ||||
| chr11:111912875-111913470 | Common:3; Rare:133 |