| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65188446-65188747 | Rare:113; Clinvar (pathogenic):1 | ||||
| chr11:65206439-65206814 | Rare:118; Clinvar:1 | ||||
| chr11:65209269-65209388 | Rare:36 | ||||
| chr11:65261737-65262046 | Common:4; Rare:90 | ||||
| chr11:65314711-65314945 | Rare:82 | ||||
| chr11:65333763-65333918 | Common:1; Rare:76 | ||||
| chr11:65558181-65558438 | Rare:56 | ||||
| chr11:65570297-65570519 | Rare:86 | ||||
| chr11:65572246-65572681 | Common:1; Rare:128 | ||||
| chr11:65575841-65576122 | Common:3; Rare:83 | ||||
| chr11:65614165-65614384 | Rare:48 | ||||
| chr11:65615288-65615652 | Common:1; Rare:130 | ||||
| chr11:65616044-65616187 | Rare:43 | ||||
| chr11:65647328-65647411 | Rare:22 | ||||
| chr11:65662658-65663081 | Common:1; Rare:105 |