| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:27506737-27506868 | Common:1; Rare:57 | ||||
| chr11:28108115-28108421 | Common:1; Rare:94 | ||||
| chr11:30016968-30017086 | Rare:33 | ||||
| chr11:30323002-30323168 | Common:1; Rare:50 | ||||
| chr11:31369713-31369882 | Rare:52 | ||||
| chr11:31509575-31509827 | Common:1; Rare:89 | ||||
| chr11:33161456-33161643 | Common:6; Rare:50 | ||||
| chr11:33257191-33257417 | Common:2; Rare:76 | ||||
| chr11:33736404-33736602 | Common:1; Rare:64 | ||||
| chr11:34438763-34439015 | Common:2; Rare:84; Clinvar (benign):1 | ||||
| chr11:34624158-34624270 | Rare:25 | ||||
| chr11:34916292-34916669 | Common:10; Rare:154; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139340 | Common:1; Rare:105 | ||||
| chr11:36510236-36510377 | Rare:40 | ||||
| chr11:43358802-43358983 | Rare:86 |