| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65638070-65638159 | Common:2; Rare:36 | ||||
| chr11:65662828-65663475 | Common:5; Rare:155 | ||||
| chr11:65711869-65712053 | Rare:59 | ||||
| chr11:65720468-65720588 | Common:1; Rare:66 | ||||
| chr11:65786834-65787099 | Common:2; Rare:38 | ||||
| chr11:65856946-65857356 | Common:4; Rare:124 | ||||
| chr11:65860172-65860459 | Common:1; Rare:94 | ||||
| chr11:65873557-65873849 | Common:3; Rare:91 | ||||
| chr11:65888407-65888686 | Common:1; Rare:97 | ||||
| chr11:65890448-65890730 | Common:4; Rare:92 | ||||
| chr11:65900389-65900745 | Common:3; Rare:78 | ||||
| chr11:65918956-65919220 | Common:2; Rare:114 | ||||
| chr11:65919652-65920155 | Common:1; Rare:172 | ||||
| chr11:65961626-65961773 | Rare:50 | ||||
| chr11:66002102-66002392 | Common:3; Rare:87; Clinvar:5; Clinvar (benign):3 |