| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74170843-74171380 | Common:3; Rare:169 | ||||
| chr11:74398373-74398581 | Common:3; Rare:51 | ||||
| chr11:74949045-74949319 | Common:6; Rare:79 | ||||
| chr11:75351696-75352004 | Common:5; Rare:87 | ||||
| chr11:75352040-75352128 | Rare:15 | ||||
| chr11:75562029-75562303 | Common:1; Rare:68; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:75668579-75669020 | Rare:104 | ||||
| chr11:76444598-76445124 | Common:1; Rare:128 | ||||
| chr11:76783048-76783395 | Common:10; Rare:113 | ||||
| chr11:76860732-76860971 | Common:3; Rare:86 | ||||
| chr11:77473562-77473770 | Common:1; Rare:74 | ||||
| chr11:77637637-77637868 | Common:1; Rare:79 | ||||
| chr11:77820686-77820936 | Common:1; Rare:74 | ||||
| chr11:77820983-77821210 | Common:1; Rare:70 | ||||
| chr11:78139590-78139809 | Common:3; Rare:88; Clinvar:2 |