| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74949079-74949288 | Common:6; Rare:54 | ||||
| chr11:76380926-76381228 | Rare:90 | ||||
| chr11:76783060-76783357 | Common:9; Rare:96 | ||||
| chr11:77820577-77820794 | Rare:81 | ||||
| chr11:77820989-77821155 | Common:1; Rare:45 | ||||
| chr11:78079807-78079934 | Common:2; Rare:43 | ||||
| chr11:83071803-83072090 | Common:4; Rare:77 | ||||
| chr11:83193661-83193780 | Common:1; Rare:50 | ||||
| chr11:83285931-83286087 | Common:3; Rare:66 | ||||
| chr11:85627231-85627427 | Common:1; Rare:37 | ||||
| chr11:85628399-85628608 | Common:3; Rare:59 | ||||
| chr11:86244971-86245262 | Common:1; Rare:126 | ||||
| chr11:86955391-86955600 | Common:1; Rare:65 | ||||
| chr11:87037770-87038043 | Common:3; Rare:127 | ||||
| chr11:88337727-88337888 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):2 |