| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35525603-35525752 | Rare:39 | ||||
| chr11:36510199-36510377 | Rare:56 | ||||
| chr11:43358794-43359012 | Rare:105 | ||||
| chr11:43880715-43880894 | Common:2; Rare:44 | ||||
| chr11:44096139-44096242 | Rare:34 | ||||
| chr11:45804258-45804468 | Common:1; Rare:46 | ||||
| chr11:45804944-45805193 | Common:3; Rare:63; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:46120949-46121033 | Rare:8 | ||||
| chr11:46121126-46121259 | Common:2; Rare:23 | ||||
| chr11:46617165-46617596 | Common:5; Rare:121 | ||||
| chr11:46700532-46700831 | Common:1; Rare:75 | ||||
| chr11:46846213-46846412 | Common:1; Rare:54 | ||||
| chr11:47176815-47177222 | Common:1; Rare:169 | ||||
| chr11:47214832-47215130 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248774-47248941 | Rare:66 |