| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47553028-47553387 | Common:2; Rare:124 | ||||
| chr11:47565434-47565918 | Common:5; Rare:132 | ||||
| chr11:47566039-47566268 | Rare:35 | ||||
| chr11:47578568-47578734 | Rare:45 | ||||
| chr11:47578914-47579148 | Rare:121; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642036-47642247 | Rare:60 | ||||
| chr11:47642354-47642890 | Rare:163 | ||||
| chr11:47715213-47715422 | Common:1; Rare:47 | ||||
| chr11:47766660-47766861 | Common:1; Rare:53 | ||||
| chr11:47766912-47767738 | Common:7; Rare:270 | ||||
| chr11:47767869-47767996 | Rare:34 | ||||
| chr11:47847864-47847964 | Rare:35 | ||||
| chr11:47848275-47848477 | Common:1; Rare:107 | ||||
| chr11:47848496-47848694 | Common:3; Rare:44 | ||||
| chr11:47980335-47980627 | Common:2; Rare:105 |