| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:76444584-76445093 | Common:2; Rare:243 | ||||
| chr11:76782710-76782950 | Common:4; Rare:75 | ||||
| chr11:76783012-76783403 | Common:20; Rare:241 | ||||
| chr11:76783430-76783600 | Common:3; Rare:57 | ||||
| chr11:76783807-76784207 | Common:18; Rare:238 | ||||
| chr11:76860660-76861010 | Common:7; Rare:199 | ||||
| chr11:77411859-77412108 | Common:3; Rare:110 | ||||
| chr11:77589350-77589750 | Common:5; Rare:191 | ||||
| chr11:77637568-77637893 | Common:2; Rare:185 | ||||
| chr11:77819810-77820722 | Common:7; Rare:392 | ||||
| chr11:77820811-77821227 | Common:3; Rare:202 | ||||
| chr11:77994633-77995080 | Common:3; Rare:195 | ||||
| chr11:78079604-78079957 | Common:6; Rare:183 | ||||
| chr11:78139469-78139858 | Common:7; Rare:250; Clinvar:6; Clinvar (benign):1 | ||||
| chr11:78188586-78188954 | Common:5; Rare:187 |