| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47565389-47565620 | Common:3; Rare:41 | ||||
| chr11:47578632-47579112 | Common:1; Rare:163; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47594409-47594545 | Common:1; Rare:41 | ||||
| chr11:47642443-47642839 | Rare:140 | ||||
| chr11:47767266-47767717 | Common:1; Rare:147 | ||||
| chr11:47848291-47848410 | Common:1; Rare:67 | ||||
| chr11:57324869-57325173 | Common:2; Rare:99 | ||||
| chr11:57335543-57335971 | Common:7; Rare:87 | ||||
| chr11:57530682-57530855 | Common:1; Rare:42 | ||||
| chr11:57560202-57560348 | Common:1; Rare:39 | ||||
| chr11:57567612-57567736 | Rare:42 | ||||
| chr11:57567829-57568091 | Common:2; Rare:48 | ||||
| chr11:57568197-57568491 | Common:1; Rare:53 | ||||
| chr11:57649751-57650081 | Common:1; Rare:66 | ||||
| chr11:57657522-57657811 | Common:4; Rare:71 |