| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47215160-47215520 | Rare:140 | ||||
| chr11:47248774-47248979 | Rare:147 | ||||
| chr11:47249010-47249470 | Common:2; Rare:122 | ||||
| chr11:47257564-47258025 | Rare:147 | ||||
| chr11:47269074-47269411 | Common:2; Rare:133 | ||||
| chr11:47269501-47269838 | Common:2; Rare:182 | ||||
| chr11:47269948-47270213 | Common:2; Rare:176 | ||||
| chr11:47408339-47408655 | Common:4; Rare:193; Clinvar (benign):4 | ||||
| chr11:47426400-47426648 | Common:2; Rare:123 | ||||
| chr11:47552849-47553211 | Common:7; Rare:242 | ||||
| chr11:47565278-47565674 | Common:6; Rare:121 | ||||
| chr11:47578550-47578860 | Rare:117 | ||||
| chr11:47578910-47579277 | Rare:285; Clinvar:4; Clinvar (pathogenic):2 | ||||
| chr11:47642390-47642821 | Rare:274 | ||||
| chr11:47715338-47715442 | Common:1; Rare:29 |