| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34052079-34052452 | Common:5; Rare:172 | ||||
| chr11:34105478-34105691 | Common:2; Rare:72 | ||||
| chr11:34438776-34438995 | Common:2; Rare:72; Clinvar (benign):1 | ||||
| chr11:34916318-34916676 | Common:10; Rare:145; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139354 | Common:1; Rare:111 | ||||
| chr11:35219093-35219387 | Common:2; Rare:68 | ||||
| chr11:35943927-35944110 | Common:3; Rare:62 | ||||
| chr11:36510229-36510362 | Rare:40 | ||||
| chr11:43358861-43359005 | Rare:73 | ||||
| chr11:45847210-45847521 | Common:2; Rare:131 | ||||
| chr11:46120952-46121259 | Common:2; Rare:46 | ||||
| chr11:46617210-46617594 | Common:5; Rare:105 | ||||
| chr11:46700549-46700818 | Common:1; Rare:70 | ||||
| chr11:47176849-47177126 | Common:1; Rare:113 | ||||
| chr11:47269981-47270184 | Common:1; Rare:68 |