| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65720750-65720852 | Rare:37; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:65780767-65781079 | Common:1; Rare:110 | ||||
| chr11:65786893-65787100 | Common:2; Rare:23 | ||||
| chr11:65857236-65857359 | Rare:39 | ||||
| chr11:65858108-65858426 | Common:2; Rare:112 | ||||
| chr11:65859269-65859737 | Rare:115 | ||||
| chr11:65860263-65861055 | Common:4; Rare:282 | ||||
| chr11:65873548-65873716 | Common:3; Rare:52 | ||||
| chr11:65888398-65888638 | Common:1; Rare:87 | ||||
| chr11:65889008-65889109 | Common:1; Rare:17 | ||||
| chr11:65890447-65890696 | Common:4; Rare:80 | ||||
| chr11:65900310-65900669 | Common:6; Rare:79 | ||||
| chr11:65917806-65917969 | Common:2; Rare:47 | ||||
| chr11:65919029-65919458 | Rare:159 | ||||
| chr11:65961467-65961797 | Common:1; Rare:111 |