| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66021108-66021257 | Rare:43; Clinvar:1 | ||||
| chr11:66289138-66289393 | Rare:54 | ||||
| chr11:66480239-66480446 | Common:1; Rare:55 | ||||
| chr11:66616398-66616648 | Common:1; Rare:67 | ||||
| chr11:66843334-66843455 | Common:5; Rare:62 | ||||
| chr11:67239769-67240058 | Common:1; Rare:67 | ||||
| chr11:67288445-67288636 | Rare:39 | ||||
| chr11:67353477-67353899 | Common:2; Rare:101 | ||||
| chr11:67428333-67428532 | Rare:70 | ||||
| chr11:67443458-67443731 | Common:2; Rare:91 | ||||
| chr11:67469166-67469454 | Common:3; Rare:101 | ||||
| chr11:67482936-67483184 | Rare:56; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508063-67508276 | Common:1; Rare:55 | ||||
| chr11:68004046-68004416 | Common:2; Rare:96 | ||||
| chr11:68010112-68010367 | Common:1; Rare:69 |