| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33161435-33161682 | Common:6; Rare:70 | ||||
| chr11:33736404-33736553 | Common:1; Rare:52 | ||||
| chr11:34052126-34052474 | Common:4; Rare:161 | ||||
| chr11:34105402-34105717 | Common:4; Rare:101 | ||||
| chr11:34916311-34916653 | Common:10; Rare:139; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35525585-35525726 | Rare:43 | ||||
| chr11:35525729-35525766 | Rare:6 | ||||
| chr11:35525769-35525821 | Rare:7 | ||||
| chr11:35526028-35526105 | Common:2; Rare:19 | ||||
| chr11:35943906-35944110 | Common:3; Rare:65 | ||||
| chr11:36289374-36289517 | Common:2; Rare:57 | ||||
| chr11:36510249-36510372 | Rare:33 | ||||
| chr11:36594378-36594581 | Common:2; Rare:40 | ||||
| chr11:43358831-43358979 | Rare:73 | ||||
| chr11:43644128-43644249 | Common:1; Rare:18 |