| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64810515-64810821 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65014028-65014252 | Rare:56 | ||||
| chr11:65084028-65084272 | Common:1; Rare:72 | ||||
| chr11:65134480-65134591 | Common:1; Rare:28 | ||||
| chr11:65181281-65181389 | Common:1; Rare:26 | ||||
| chr11:65314717-65314906 | Rare:68 | ||||
| chr11:65333602-65333881 | Common:1; Rare:117 | ||||
| chr11:65386480-65386684 | Common:1; Rare:65 | ||||
| chr11:65504051-65504869 | Common:3; Rare:391 | ||||
| chr11:65570335-65570494 | Rare:63 | ||||
| chr11:65614179-65614231 | Rare:18 | ||||
| chr11:65614238-65614484 | Rare:50 | ||||
| chr11:65662895-65663099 | Common:1; Rare:50 | ||||
| chr11:65711869-65712051 | Rare:59 | ||||
| chr11:65856952-65857076 | Common:3; Rare:41 |