| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322496-18322608 | Common:2; Rare:50 | ||||
| chr11:18394397-18394626 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr11:18396204-18396390 | Rare:67 | ||||
| chr11:18526851-18526987 | Rare:66 | ||||
| chr11:20387505-20387743 | Common:4; Rare:75 | ||||
| chr11:22625799-22625938 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:27506748-27506852 | Common:1; Rare:44 | ||||
| chr11:28108115-28108414 | Common:1; Rare:90 | ||||
| chr11:30322988-30323154 | Common:1; Rare:48 | ||||
| chr11:31369737-31369877 | Rare:45 | ||||
| chr11:31509575-31509787 | Common:1; Rare:65 | ||||
| chr11:33015754-33015929 | Common:2; Rare:69 | ||||
| chr11:33161435-33161657 | Common:6; Rare:60 | ||||
| chr11:34916287-34916650 | Common:9; Rare:148; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr11:35943940-35944081 | Common:2; Rare:50 |