| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66677550-66678241 | Common:1; Rare:219 | ||||
| chr11:66728353-66728486 | Rare:34 | ||||
| chr11:66744486-66744826 | Common:2; Rare:118 | ||||
| chr11:66744850-66745011 | Common:1; Rare:32 | ||||
| chr11:66745116-66745216 | Rare:29 | ||||
| chr11:66842927-66843106 | Common:1; Rare:75 | ||||
| chr11:66843229-66843542 | Common:6; Rare:163 | ||||
| chr11:66843593-66843700 | Rare:43 | ||||
| chr11:66856127-66856646 | Common:1; Rare:163 | ||||
| chr11:66856660-66856910 | Common:1; Rare:64 | ||||
| chr11:66856963-66857233 | Rare:85 | ||||
| chr11:66957881-66958234 | Common:3; Rare:94 | ||||
| chr11:66958284-66958920 | Common:6; Rare:173; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:67006628-67006845 | Common:2; Rare:56 | ||||
| chr11:67023576-67023615 | Rare:9 |