| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35138954-35139339 | Common:1; Rare:104 | ||||
| chr11:35943981-35944109 | Common:1; Rare:40 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358844-43359001 | Rare:76 | ||||
| chr11:43880776-43881109 | Common:5; Rare:75 | ||||
| chr11:46345236-46345450 | Common:1; Rare:67 | ||||
| chr11:46617210-46617585 | Common:5; Rare:103 | ||||
| chr11:46700568-46700818 | Common:1; Rare:64 | ||||
| chr11:46700950-46701074 | Common:1; Rare:40 | ||||
| chr11:46846207-46846416 | Common:1; Rare:61 | ||||
| chr11:47176846-47177152 | Common:1; Rare:125 | ||||
| chr11:47214837-47215123 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248791-47248955 | Rare:69 | ||||
| chr11:47269545-47269690 | Common:1; Rare:50 | ||||
| chr11:47269981-47270184 | Common:1; Rare:68 |