| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64240888-64241179 | Rare:78 | ||||
| chr11:64241385-64241673 | Rare:59 | ||||
| chr11:64270094-64270520 | Common:1; Rare:179 | ||||
| chr11:64284534-64284819 | Rare:113 | ||||
| chr11:64317462-64317612 | Common:3; Rare:61 | ||||
| chr11:64318035-64318299 | Rare:117 | ||||
| chr11:64359060-64359224 | Rare:36 | ||||
| chr11:64759842-64760079 | Rare:66; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr11:64778757-64779003 | Common:3; Rare:81 | ||||
| chr11:64854783-64854932 | Rare:44 | ||||
| chr11:64917177-64917573 | Common:3; Rare:92 | ||||
| chr11:64924569-64924700 | Rare:34 | ||||
| chr11:65014019-65014235 | Rare:59 | ||||
| chr11:65084028-65084272 | Common:1; Rare:72 | ||||
| chr11:65134480-65134579 | Common:1; Rare:25 |