| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18634268-18634567 | Common:3; Rare:106 | ||||
| chr11:18706450-18706524 | Rare:15 | ||||
| chr11:19714077-19714195 | Rare:26 | ||||
| chr11:19931254-19931565 | Common:3; Rare:72 | ||||
| chr11:20387488-20387777 | Common:5; Rare:91 | ||||
| chr11:22625801-22626002 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:22829343-22829440 | Common:1; Rare:27 | ||||
| chr11:22829713-22829781 | Common:1; Rare:30 | ||||
| chr11:27506717-27506865 | Common:1; Rare:69 | ||||
| chr11:27700167-27700299 | Common:1; Rare:22 | ||||
| chr11:28108096-28108429 | Common:1; Rare:99 | ||||
| chr11:30322944-30323217 | Common:3; Rare:75 | ||||
| chr11:30328444-30328702 | Common:2; Rare:39 | ||||
| chr11:31369723-31369915 | Rare:57 | ||||
| chr11:31509570-31509820 | Common:1; Rare:83 |