| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:81752660-81752821 | Rare:81 | ||||
| chr6:83193194-83193397 | Common:3; Rare:69 | ||||
| chr6:85449521-85449732 | Common:1; Rare:52 | ||||
| chr6:85449905-85450150 | Common:1; Rare:73 | ||||
| chr6:85593734-85593975 | Common:1; Rare:83 | ||||
| chr6:85643817-85643931 | Common:2; Rare:36 | ||||
| chr6:87155248-87155594 | Rare:90 | ||||
| chr6:87472832-87473006 | Common:1; Rare:60; Clinvar (benign):4 | ||||
| chr6:87589940-87590165 | Common:2; Rare:105; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87702189-87702505 | Common:2; Rare:100 | ||||
| chr6:88963569-88963830 | Common:2; Rare:87 | ||||
| chr6:89080606-89080784 | Common:1; Rare:77 | ||||
| chr6:89081039-89081411 | Common:2; Rare:141 | ||||
| chr6:89081948-89082045 | Common:1; Rare:21 | ||||
| chr6:89117944-89118085 | Common:1; Rare:56 |