| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67239832-67240146 | Rare:68 | ||||
| chr11:67353444-67353779 | Common:2; Rare:82 | ||||
| chr11:67401783-67402075 | Common:3; Rare:109 | ||||
| chr11:67428340-67428531 | Rare:65 | ||||
| chr11:67443458-67443702 | Common:2; Rare:85 | ||||
| chr11:67469229-67469407 | Common:1; Rare:52 | ||||
| chr11:67482913-67483185 | Rare:61; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508637-67508778 | Common:3; Rare:51 | ||||
| chr11:68030367-68030744 | Common:3; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038919-68039060 | Rare:42; Clinvar:1 | ||||
| chr11:68271862-68272108 | Common:2; Rare:99 | ||||
| chr11:68460538-68460773 | Common:3; Rare:91 | ||||
| chr11:68903764-68903961 | Common:5; Rare:92; Clinvar:3; Clinvar (benign):7 | ||||
| chr11:69048748-69048944 | Common:5; Rare:67 | ||||
| chr11:69640983-69641222 | Rare:51 |