| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67401733-67402075 | Common:3; Rare:125 | ||||
| chr11:67428336-67428566 | Rare:86 | ||||
| chr11:67443458-67443639 | Common:1; Rare:66 | ||||
| chr11:67452286-67452416 | Common:1; Rare:55 | ||||
| chr11:67469205-67469407 | Common:1; Rare:66 | ||||
| chr11:67482936-67483183 | Rare:56; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508002-67508199 | Common:1; Rare:64 | ||||
| chr11:67508615-67508787 | Common:3; Rare:61 | ||||
| chr11:67583568-67583876 | Common:2; Rare:97 | ||||
| chr11:68010112-68010380 | Common:1; Rare:69 | ||||
| chr11:68014821-68014955 | Rare:27 | ||||
| chr11:68030432-68030744 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038919-68039116 | Rare:59; Clinvar:1 | ||||
| chr11:68049381-68049783 | Common:2; Rare:129; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr11:68213553-68213941 | Common:1; Rare:224 |