| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:27506729-27506852 | Common:1; Rare:59 | ||||
| chr11:28108134-28108414 | Common:1; Rare:82 | ||||
| chr11:30584198-30584337 | Common:1; Rare:18 | ||||
| chr11:31369728-31369887 | Rare:49 | ||||
| chr11:31509561-31509790 | Common:1; Rare:72 | ||||
| chr11:31811217-31811492 | Rare:48; Clinvar:2 | ||||
| chr11:31812185-31812446 | Common:5; Rare:46 | ||||
| chr11:31816364-31816581 | Common:2; Rare:55 | ||||
| chr11:31817904-31817918 | Rare:2 | ||||
| chr11:31817920-31818085 | Common:2; Rare:51 | ||||
| chr11:33161449-33161629 | Common:6; Rare:48 | ||||
| chr11:33774493-33774670 | Common:2; Rare:62 | ||||
| chr11:34916318-34916664 | Common:10; Rare:140; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35943939-35944127 | Common:2; Rare:65 | ||||
| chr11:36510229-36510372 | Rare:43 |