| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69048747-69048944 | Common:5; Rare:67 | ||||
| chr11:69640972-69641172 | Rare:40 | ||||
| chr11:69675289-69675491 | Rare:59 | ||||
| chr11:70203124-70203313 | Common:3; Rare:74 | ||||
| chr11:70398349-70398596 | Common:2; Rare:86 | ||||
| chr11:70826695-70826722 | Rare:1 | ||||
| chr11:71448338-71448703 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71453029-71453258 | Common:1; Rare:66 | ||||
| chr11:71928940-71929058 | Common:1; Rare:42 | ||||
| chr11:72039789-72039815 | Rare:2 | ||||
| chr11:72039823-72039873 | Common:1; Rare:4 | ||||
| chr11:72041015-72041295 | Common:1; Rare:55 | ||||
| chr11:72041531-72041724 | Rare:28 | ||||
| chr11:72041846-72041911 | Common:2; Rare:11 | ||||
| chr11:72041920-72041995 | Rare:13 |