| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358845-43358983 | Rare:65 | ||||
| chr11:43680439-43680761 | Common:2; Rare:76 | ||||
| chr11:44066195-44066335 | Common:1; Rare:33 | ||||
| chr11:45804311-45804427 | Common:1; Rare:25 | ||||
| chr11:45847210-45847487 | Common:2; Rare:111 | ||||
| chr11:45917837-45918190 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46120948-46121312 | Common:2; Rare:57 | ||||
| chr11:46617238-46617585 | Common:5; Rare:97 | ||||
| chr11:47176849-47177131 | Common:1; Rare:115 | ||||
| chr11:47186408-47186495 | Rare:27 | ||||
| chr11:47214866-47215110 | Common:1; Rare:62; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47269550-47269714 | Common:1; Rare:56 | ||||
| chr11:47269983-47270172 | Common:1; Rare:65 | ||||
| chr11:47426423-47426639 | Rare:54 |