| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65314685-65314921 | Rare:76 | ||||
| chr11:65333762-65333908 | Common:1; Rare:75 | ||||
| chr11:65386480-65386690 | Common:1; Rare:66 | ||||
| chr11:65570335-65570498 | Rare:66 | ||||
| chr11:65614198-65614394 | Rare:40 | ||||
| chr11:65662877-65663093 | Common:1; Rare:57 | ||||
| chr11:65711869-65712042 | Rare:53 | ||||
| chr11:65856952-65857334 | Common:4; Rare:114 | ||||
| chr11:65860182-65860436 | Common:1; Rare:85 | ||||
| chr11:65888407-65888640 | Common:1; Rare:86 | ||||
| chr11:65890502-65890703 | Common:3; Rare:70 | ||||
| chr11:65900381-65900459 | Common:1; Rare:14 | ||||
| chr11:65961547-65961764 | Rare:76 | ||||
| chr11:66002127-66002356 | Common:3; Rare:68; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:66002456-66002777 | Common:1; Rare:83; Clinvar:1 |