| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64759845-64760193 | Rare:83; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr11:64778757-64778961 | Common:2; Rare:70 | ||||
| chr11:64803127-64803375 | Rare:101 | ||||
| chr11:64878480-64878856 | Common:4; Rare:146 | ||||
| chr11:65014020-65014268 | Rare:64 | ||||
| chr11:65084017-65084272 | Common:1; Rare:76 | ||||
| chr11:65110587-65110736 | Rare:40 | ||||
| chr11:65134480-65134574 | Common:1; Rare:23 | ||||
| chr11:65181059-65181389 | Common:2; Rare:79 | ||||
| chr11:65181439-65181715 | Common:2; Rare:94 | ||||
| chr11:65293907-65294190 | Common:1; Rare:53 | ||||
| chr11:65314717-65314931 | Rare:77 | ||||
| chr11:65333617-65333898 | Common:1; Rare:119 | ||||
| chr11:65386460-65386690 | Common:1; Rare:75 | ||||
| chr11:65503816-65504269 | Common:2; Rare:228 |