| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65638011-65638153 | Common:3; Rare:64 | ||||
| chr11:65662792-65663031 | Common:2; Rare:90 | ||||
| chr11:65780875-65781067 | Rare:131 | ||||
| chr11:65856985-65857385 | Common:8; Rare:227 | ||||
| chr11:65859370-65859660 | Rare:79 | ||||
| chr11:65860328-65860681 | Common:6; Rare:194 | ||||
| chr11:65860741-65861550 | Common:5; Rare:306 | ||||
| chr11:65873491-65873951 | Common:6; Rare:183 | ||||
| chr11:65888402-65888676 | Common:2; Rare:185 | ||||
| chr11:65890453-65890772 | Common:7; Rare:185 | ||||
| chr11:65918998-65919533 | Common:2; Rare:368 | ||||
| chr11:65961475-65961809 | Common:2; Rare:210 | ||||
| chr11:65961800-65962250 | Common:8; Rare:201 | ||||
| chr11:66002086-66002563 | Common:6; Rare:233; Clinvar:15; Clinvar (benign):6 | ||||
| chr11:66002465-66002802 | Common:1; Rare:94; Clinvar:1 |