| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64809691-64810414 | Common:7; Rare:290; Clinvar:45; Clinvar (benign):39; Clinvar (pathogenic):6 | ||||
| chr11:64810471-64810872 | Common:20; Rare:494; Clinvar:6; Clinvar (benign):12 | ||||
| chr11:64843892-64844292 | Common:2; Rare:85 | ||||
| chr11:64844472-64845379 | Common:27; Rare:796 | ||||
| chr11:64854470-64855342 | Common:6; Rare:456 | ||||
| chr11:64856588-64856988 | Common:3; Rare:68 | ||||
| chr11:64878390-64878930 | Common:23; Rare:847 | ||||
| chr11:64879286-64879415 | Common:2; Rare:18 | ||||
| chr11:64887315-64888220 | Common:6; Rare:448 | ||||
| chr11:64888579-64888979 | Common:6; Rare:79 | ||||
| chr11:64917001-64918244 | Common:26; Rare:917 | ||||
| chr11:64923629-64924374 | Common:4; Rare:220 | ||||
| chr11:64924429-64924840 | Common:5; Rare:334 | ||||
| chr11:64971911-64972391 | Common:10; Rare:604 | ||||
| chr11:64990095-64990601 | Common:5; Rare:205 |