| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66466394-66466479 | Common:1; Rare:20 | ||||
| chr11:66466633-66467012 | Rare:120 | ||||
| chr11:66467090-66467175 | Rare:12 | ||||
| chr11:66467237-66467342 | Common:1; Rare:18 | ||||
| chr11:66479911-66480071 | Rare:26 | ||||
| chr11:66480141-66480478 | Common:3; Rare:93 | ||||
| chr11:66510532-66510741 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr11:66545974-66546239 | Common:4; Rare:71 | ||||
| chr11:66568525-66568653 | Common:1; Rare:42 | ||||
| chr11:66593016-66593273 | Common:1; Rare:90 | ||||
| chr11:66616107-66616776 | Common:2; Rare:196 | ||||
| chr11:66616824-66617056 | Rare:58 | ||||
| chr11:66638260-66638819 | Common:4; Rare:227 | ||||
| chr11:66638886-66639129 | Rare:71 | ||||
| chr11:66639276-66639637 | Common:1; Rare:102 |