| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66002458-66002819 | Common:1; Rare:100; Clinvar:1 | ||||
| chr11:66070838-66070951 | Rare:30 | ||||
| chr11:66257609-66257828 | Rare:61 | ||||
| chr11:66258403-66258596 | Rare:53 | ||||
| chr11:66268404-66268692 | Common:3; Rare:83 | ||||
| chr11:66289064-66289393 | Common:1; Rare:80 | ||||
| chr11:66345049-66345203 | Common:1; Rare:43 | ||||
| chr11:66347557-66347869 | Common:5; Rare:76; Clinvar (benign):1 | ||||
| chr11:66466694-66466987 | Rare:89 | ||||
| chr11:66480211-66480452 | Common:3; Rare:65 | ||||
| chr11:66567254-66567470 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:66568317-66568415 | Common:1; Rare:22; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:66593081-66593258 | Common:1; Rare:65 | ||||
| chr11:66616408-66616646 | Common:1; Rare:62 | ||||
| chr11:66638393-66638751 | Common:4; Rare:156 |