| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64778413-64778698 | Common:2; Rare:132 | ||||
| chr11:64810508-64810642 | Common:2; Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:65014028-65014252 | Rare:56 | ||||
| chr11:65084012-65084272 | Common:1; Rare:79 | ||||
| chr11:65096064-65096259 | Common:1; Rare:57 | ||||
| chr11:65109419-65109722 | Common:1; Rare:85 | ||||
| chr11:65134507-65134571 | Common:1; Rare:11 | ||||
| chr11:65181248-65181704 | Common:3; Rare:135 | ||||
| chr11:65181857-65181995 | Rare:27 | ||||
| chr11:65261772-65261941 | Common:1; Rare:48 | ||||
| chr11:65314717-65314902 | Rare:66 | ||||
| chr11:65333617-65333881 | Common:1; Rare:113 | ||||
| chr11:65386480-65386657 | Common:1; Rare:53 | ||||
| chr11:65524858-65525138 | Rare:48 | ||||
| chr11:65570328-65570506 | Rare:71 |