| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:83193183-83193423 | Common:3; Rare:79 | ||||
| chr6:83707931-83708073 | Rare:36 | ||||
| chr6:83853003-83853385 | Common:2; Rare:88 | ||||
| chr6:83853483-83853709 | Common:2; Rare:77 | ||||
| chr6:83859561-83859742 | Rare:66 | ||||
| chr6:84227584-84227999 | Common:4; Rare:103 | ||||
| chr6:85449932-85450146 | Common:1; Rare:65 | ||||
| chr6:85593714-85594063 | Common:2; Rare:113 | ||||
| chr6:85642803-85643049 | Common:2; Rare:93 | ||||
| chr6:85643812-85644044 | Common:2; Rare:73 | ||||
| chr6:87152285-87152618 | Common:4; Rare:66 | ||||
| chr6:87155154-87155637 | Common:1; Rare:137 | ||||
| chr6:87408429-87408652 | Common:1; Rare:45 | ||||
| chr6:87472882-87473004 | Common:1; Rare:46; Clinvar (benign):4 | ||||
| chr6:87589885-87590180 | Common:3; Rare:158; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 |