| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62621901-62622375 | Common:4; Rare:136 | ||||
| chr11:62646150-62646352 | Common:3; Rare:58 | ||||
| chr11:62646518-62646817 | Common:1; Rare:124; Clinvar (pathogenic):1 | ||||
| chr11:62653132-62653579 | Common:1; Rare:117 | ||||
| chr11:62664714-62664936 | Common:2; Rare:63 | ||||
| chr11:62665045-62665503 | Common:6; Rare:204 | ||||
| chr11:62665601-62665638 | Common:1; Rare:9 | ||||
| chr11:62671352-62671461 | Common:1; Rare:24 | ||||
| chr11:62671544-62672113 | Common:4; Rare:207; Clinvar (benign):5 | ||||
| chr11:62672192-62672426 | Rare:61 | ||||
| chr11:62678987-62679286 | Rare:92 | ||||
| chr11:62706158-62706484 | Common:3; Rare:119; Clinvar (benign):6 | ||||
| chr11:62709424-62709876 | Common:2; Rare:168 | ||||
| chr11:62710003-62710121 | Rare:31 | ||||
| chr11:62727038-62727507 | Common:2; Rare:199 |