| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65014040-65014241 | Rare:51 | ||||
| chr11:65084028-65084287 | Common:1; Rare:82 | ||||
| chr11:65181599-65181987 | Common:3; Rare:109 | ||||
| chr11:65314676-65314913 | Rare:73 | ||||
| chr11:65333686-65333892 | Common:1; Rare:94 | ||||
| chr11:65570340-65570504 | Rare:68 | ||||
| chr11:65616045-65616204 | Rare:50 | ||||
| chr11:65637886-65638114 | Common:1; Rare:88 | ||||
| chr11:65662902-65663007 | Common:1; Rare:29 | ||||
| chr11:65919537-65919838 | Common:1; Rare:99 | ||||
| chr11:66002127-66002521 | Common:3; Rare:107; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66289041-66289369 | Common:1; Rare:78 | ||||
| chr11:66480239-66480441 | Common:1; Rare:54 | ||||
| chr11:67443458-67443549 | Common:1; Rare:27 | ||||
| chr11:67482954-67483164 | Rare:48; Clinvar:1; Clinvar (benign):3 |