| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85449931-85450141 | Common:2; Rare:120 | ||||
| chr6:85593699-85594007 | Common:2; Rare:191 | ||||
| chr6:85642782-85643092 | Common:5; Rare:177 | ||||
| chr6:85643216-85643701 | Common:3; Rare:303 | ||||
| chr6:85643803-85643964 | Common:3; Rare:77 | ||||
| chr6:85644003-85644403 | Rare:108 | ||||
| chr6:87155226-87155621 | Rare:205 | ||||
| chr6:87472828-87473017 | Common:3; Rare:114; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:87589731-87590172 | Common:5; Rare:303; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr6:87701878-87702008 | Rare:43 | ||||
| chr6:87702121-87702489 | Common:6; Rare:222 | ||||
| chr6:88963490-88963889 | Common:4; Rare:219 | ||||
| chr6:89080586-89081051 | Common:4; Rare:272 | ||||
| chr6:89145410-89145740 | Common:2; Rare:90 | ||||
| chr6:89145888-89146183 | Rare:153 |