| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33074247-33074303 | Common:1; Rare:5 | ||||
| chr11:33161398-33161678 | Common:6; Rare:75 | ||||
| chr11:33736390-33736605 | Common:2; Rare:66 | ||||
| chr11:34051626-34051766 | Rare:59 | ||||
| chr11:34916311-34916658 | Common:10; Rare:141; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:36510236-36510353 | Rare:33 | ||||
| chr11:46120948-46121009 | Rare:5 | ||||
| chr11:46121041-46121338 | Common:2; Rare:52 | ||||
| chr11:46617175-46617585 | Common:5; Rare:114 | ||||
| chr11:46700563-46700769 | Common:1; Rare:50 | ||||
| chr11:46846148-46846421 | Common:1; Rare:88 | ||||
| chr11:47248791-47248943 | Rare:62 | ||||
| chr11:47565478-47565621 | Common:3; Rare:29 | ||||
| chr11:47578944-47579334 | Rare:181; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:47638735-47639032 | Common:5; Rare:78 |