| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62646574-62646772 | Common:1; Rare:80; Clinvar (pathogenic):1 | ||||
| chr11:62665055-62665418 | Common:5; Rare:164 | ||||
| chr11:62679006-62679190 | Rare:60 | ||||
| chr11:62706231-62706428 | Common:2; Rare:90; Clinvar (benign):4 | ||||
| chr11:62707179-62707737 | Common:5; Rare:125 | ||||
| chr11:62709501-62709659 | Rare:72 | ||||
| chr11:62728418-62728518 | Common:1; Rare:61 | ||||
| chr11:62754115-62754402 | Common:1; Rare:70 | ||||
| chr11:62761394-62761608 | Common:1; Rare:56 | ||||
| chr11:62771213-62771454 | Rare:68 | ||||
| chr11:62832015-62832250 | Rare:84 | ||||
| chr11:62841805-62842103 | Common:6; Rare:123 | ||||
| chr11:62855881-62856169 | Rare:106 | ||||
| chr11:62880792-62880935 | Rare:41 | ||||
| chr11:62881464-62881815 | Common:4; Rare:80 |