| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65615731-65615830 | Rare:37 | ||||
| chr11:65616023-65616191 | Rare:49 | ||||
| chr11:65647294-65647391 | Rare:28 | ||||
| chr11:65662895-65663081 | Common:1; Rare:47 | ||||
| chr11:65720491-65720578 | Common:1; Rare:47 | ||||
| chr11:65856982-65857329 | Common:4; Rare:104 | ||||
| chr11:65860172-65860840 | Common:3; Rare:222 | ||||
| chr11:65888365-65888676 | Common:1; Rare:104 | ||||
| chr11:65900225-65900612 | Common:5; Rare:90 | ||||
| chr11:65976377-65976762 | Rare:111 | ||||
| chr11:66002083-66002406 | Common:3; Rare:96; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:66002454-66002834 | Common:1; Rare:105; Clinvar:1 | ||||
| chr11:66058024-66058411 | Rare:100 | ||||
| chr11:66268701-66268866 | Common:2; Rare:59 | ||||
| chr11:66288990-66289396 | Common:1; Rare:100 |