| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62547200-62547410 | Rare:86 | ||||
| chr11:62591459-62591840 | Rare:255 | ||||
| chr11:62611380-62611820 | Rare:223 | ||||
| chr11:62612441-62612905 | Common:9; Rare:222; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:62621934-62622225 | Common:4; Rare:177 | ||||
| chr11:62646571-62646817 | Common:2; Rare:179; Clinvar (pathogenic):1 | ||||
| chr11:62653236-62653413 | Common:1; Rare:64 | ||||
| chr11:62665055-62665396 | Common:10; Rare:278 | ||||
| chr11:62679018-62679239 | Rare:116 | ||||
| chr11:62724090-62724578 | Common:3; Rare:160 | ||||
| chr11:62727058-62727293 | Common:3; Rare:151 | ||||
| chr11:62727368-62727729 | Common:1; Rare:289 | ||||
| chr11:62727894-62728187 | Common:12; Rare:149 | ||||
| chr11:62754136-62754431 | Common:3; Rare:103 | ||||
| chr11:62787292-62787488 | Common:4; Rare:221 |