| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45917793-45917953 | Rare:44 | ||||
| chr11:45917997-45918266 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr11:45918736-45918851 | Common:1; Rare:30 | ||||
| chr11:45922296-45922722 | Common:8; Rare:130 | ||||
| chr11:46119231-46119323 | Rare:16 | ||||
| chr11:46119416-46119646 | Common:1; Rare:46 | ||||
| chr11:46119794-46119969 | Common:2; Rare:51 | ||||
| chr11:46120018-46120089 | Common:1; Rare:8 | ||||
| chr11:46120102-46120165 | Rare:11 | ||||
| chr11:46120464-46120796 | Rare:68 | ||||
| chr11:46120868-46121043 | Rare:22 | ||||
| chr11:46121080-46121742 | Common:2; Rare:155 | ||||
| chr11:46295589-46295668 | Rare:36 | ||||
| chr11:46347220-46347635 | Common:2; Rare:133 | ||||
| chr11:46347886-46348066 | Rare:39 |