| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65181617-65182003 | Common:3; Rare:105 | ||||
| chr11:65314726-65314913 | Rare:68 | ||||
| chr11:65333766-65333901 | Common:1; Rare:70 | ||||
| chr11:65381944-65382158 | Common:3; Rare:51 | ||||
| chr11:65386460-65386684 | Common:1; Rare:74 | ||||
| chr11:65502872-65503650 | Common:3; Rare:354 | ||||
| chr11:65503663-65504188 | Common:2; Rare:256 | ||||
| chr11:65545502-65545547 | Rare:10 | ||||
| chr11:65557716-65557889 | Rare:44; Clinvar (pathogenic):1 | ||||
| chr11:65558193-65558419 | Rare:54 | ||||
| chr11:65570284-65570521 | Rare:91 | ||||
| chr11:65572246-65572580 | Rare:96 | ||||
| chr11:65575855-65576090 | Common:3; Rare:68 | ||||
| chr11:65614186-65614351 | Rare:39 | ||||
| chr11:65615340-65615377 | Rare:9 |