| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65014051-65014228 | Rare:42 | ||||
| chr11:65084073-65084272 | Common:1; Rare:57 | ||||
| chr11:65134476-65134579 | Common:1; Rare:27 | ||||
| chr11:65314717-65314902 | Rare:66 | ||||
| chr11:65386374-65386663 | Common:1; Rare:78 | ||||
| chr11:65570344-65570483 | Rare:55 | ||||
| chr11:65662890-65663208 | Common:2; Rare:72 | ||||
| chr11:65888432-65888670 | Common:1; Rare:82 | ||||
| chr11:66002122-66002561 | Common:3; Rare:125; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66268404-66268655 | Common:3; Rare:72 | ||||
| chr11:66347630-66347869 | Common:5; Rare:55 | ||||
| chr11:66480239-66480444 | Common:1; Rare:54 | ||||
| chr11:66510551-66510677 | Common:1; Rare:57; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr11:66616398-66616636 | Common:1; Rare:64 | ||||
| chr11:66677769-66677859 | Common:1; Rare:35 |