| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:83193201-83193403 | Common:3; Rare:69 | ||||
| chr6:83709071-83709363 | Common:4; Rare:87 | ||||
| chr6:83853219-83853272 | Common:1; Rare:16 | ||||
| chr6:83853483-83853663 | Common:1; Rare:52 | ||||
| chr6:84764572-84764776 | Rare:60 | ||||
| chr6:85643291-85643458 | Rare:70 | ||||
| chr6:85643817-85643941 | Common:2; Rare:39 | ||||
| chr6:87155229-87155620 | Rare:110 | ||||
| chr6:87589955-87590171 | Common:3; Rare:99; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87702215-87702485 | Common:1; Rare:84 | ||||
| chr6:88165863-88166364 | Common:3; Rare:151 | ||||
| chr6:88963540-88963773 | Rare:78 | ||||
| chr6:89117944-89118128 | Common:3; Rare:77 | ||||
| chr6:89638434-89638549 | Common:1; Rare:25 | ||||
| chr6:89638721-89638829 | Common:3; Rare:38 |