| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70398429-70398596 | Common:2; Rare:60 | ||||
| chr11:71448352-71448677 | Common:3; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71928923-71929104 | Common:1; Rare:58 | ||||
| chr11:72080449-72080847 | Common:2; Rare:89; Clinvar:7 | ||||
| chr11:73598058-73598301 | Common:2; Rare:62 | ||||
| chr11:73876799-73877024 | Common:4; Rare:58 | ||||
| chr11:73982838-73982962 | Common:6; Rare:36 | ||||
| chr11:74170853-74171367 | Common:2; Rare:162 | ||||
| chr11:74398378-74398551 | Common:3; Rare:36 | ||||
| chr11:74949071-74949364 | Common:6; Rare:89 | ||||
| chr11:76381125-76381348 | Common:3; Rare:73 | ||||
| chr11:76444660-76444919 | Rare:58 | ||||
| chr11:76783054-76783353 | Common:9; Rare:97 | ||||
| chr11:77637674-77637867 | Common:1; Rare:73 | ||||
| chr11:77820989-77821148 | Common:1; Rare:43 |