| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65382435-65382811 | Rare:70 | ||||
| chr11:65386535-65386669 | Rare:43 | ||||
| chr11:65524792-65525161 | Rare:72 | ||||
| chr11:65539850-65540041 | Common:2; Rare:75; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65540520-65540930 | Common:4; Rare:161; Clinvar:1 | ||||
| chr11:65546550-65546900 | Common:3; Rare:113; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:65552181-65552350 | Common:1; Rare:47 | ||||
| chr11:65557345-65557631 | Rare:58 | ||||
| chr11:65558171-65558472 | Common:3; Rare:67 | ||||
| chr11:65558593-65558718 | Common:3; Rare:23 | ||||
| chr11:65559252-65559478 | Common:2; Rare:44 | ||||
| chr11:65569998-65570146 | Common:1; Rare:48 | ||||
| chr11:65570165-65570510 | Common:2; Rare:116 | ||||
| chr11:65572444-65572593 | Rare:48 | ||||
| chr11:65575844-65576036 | Common:3; Rare:55 |