| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47269083-47269382 | Common:1; Rare:60 | ||||
| chr11:47269550-47269714 | Common:1; Rare:56 | ||||
| chr11:47269981-47270217 | Common:1; Rare:85 | ||||
| chr11:47426359-47426658 | Common:1; Rare:76 | ||||
| chr11:47565478-47565650 | Common:3; Rare:35 | ||||
| chr11:47578947-47579128 | Rare:97; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642464-47642799 | Rare:123 | ||||
| chr11:47767201-47767352 | Common:1; Rare:79 | ||||
| chr11:57324860-57325183 | Common:2; Rare:104 | ||||
| chr11:57426885-57427236 | Common:1; Rare:93 | ||||
| chr11:57567612-57567728 | Rare:40 | ||||
| chr11:57657455-57657821 | Common:4; Rare:91 | ||||
| chr11:57667745-57668124 | Common:4; Rare:128 | ||||
| chr11:57712163-57712671 | Common:9; Rare:175 | ||||
| chr11:57741243-57741609 | Common:1; Rare:141 |