| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33085762-33085989 | Rare:50 | ||||
| chr11:33161449-33161648 | Common:6; Rare:52 | ||||
| chr11:33257195-33257433 | Common:3; Rare:82 | ||||
| chr11:33257613-33257706 | Rare:22 | ||||
| chr11:33258536-33258631 | Rare:39 | ||||
| chr11:33736391-33736605 | Common:2; Rare:66 | ||||
| chr11:34052119-34052573 | Common:4; Rare:208 | ||||
| chr11:34105480-34105717 | Common:2; Rare:79 | ||||
| chr11:34916292-34916661 | Common:10; Rare:149; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35943923-35944143 | Common:4; Rare:70 | ||||
| chr11:36289411-36289505 | Common:1; Rare:32 | ||||
| chr11:36510236-36510372 | Rare:38 | ||||
| chr11:43358831-43358983 | Rare:76 | ||||
| chr11:44066190-44066530 | Common:3; Rare:86 | ||||
| chr11:45847252-45847505 | Common:2; Rare:100 |