| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65111657-65111885 | Rare:72 | ||||
| chr11:65122089-65122381 | Common:4; Rare:106 | ||||
| chr11:65134484-65134818 | Common:3; Rare:87 | ||||
| chr11:65181670-65182490 | Common:3; Rare:164 | ||||
| chr11:65261680-65262035 | Common:4; Rare:121 | ||||
| chr11:65314679-65314906 | Rare:70 | ||||
| chr11:65333737-65333908 | Common:1; Rare:85 | ||||
| chr11:65354496-65354791 | Common:1; Rare:88 | ||||
| chr11:65382649-65382773 | Rare:18 | ||||
| chr11:65386390-65386820 | Common:2; Rare:114 | ||||
| chr11:65524792-65525147 | Rare:69 | ||||
| chr11:65546488-65546933 | Common:9; Rare:365; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr11:65558060-65558520 | Common:3; Rare:90 | ||||
| chr11:65558540-65558960 | Common:4; Rare:79 | ||||
| chr11:65569912-65570115 | Common:1; Rare:73 |