| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:45805011-45805180 | Common:2; Rare:38; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:46617238-46617585 | Common:5; Rare:97 | ||||
| chr11:46700559-46700834 | Common:1; Rare:69 | ||||
| chr11:46846213-46846362 | Rare:37 | ||||
| chr11:47176849-47177126 | Common:1; Rare:113 | ||||
| chr11:47248793-47248938 | Rare:57 | ||||
| chr11:47269083-47269388 | Common:1; Rare:62 | ||||
| chr11:47269529-47269690 | Common:1; Rare:53 | ||||
| chr11:47269991-47270212 | Common:1; Rare:81 | ||||
| chr11:47426423-47426658 | Rare:57 | ||||
| chr11:47553031-47553356 | Common:2; Rare:115 | ||||
| chr11:47565478-47565620 | Common:3; Rare:28 | ||||
| chr11:47578675-47578772 | Rare:21 | ||||
| chr11:47578947-47579100 | Rare:80; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642461-47642668 | Rare:93 |