| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:83193222-83193395 | Common:3; Rare:62 | ||||
| chr6:85449954-85450150 | Common:1; Rare:59 | ||||
| chr6:85642853-85642982 | Rare:54 | ||||
| chr6:87155355-87155590 | Rare:67 | ||||
| chr6:87589936-87590175 | Common:3; Rare:115; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87700932-87701187 | Common:1; Rare:59 | ||||
| chr6:87701884-87702033 | Common:1; Rare:50 | ||||
| chr6:88165994-88166261 | Common:1; Rare:78 | ||||
| chr6:88963585-88963773 | Rare:65 | ||||
| chr6:89080588-89080829 | Common:1; Rare:102 | ||||
| chr6:89081007-89081378 | Common:3; Rare:145 | ||||
| chr6:89352673-89353002 | Common:1; Rare:73 | ||||
| chr6:89638434-89638541 | Common:1; Rare:24 | ||||
| chr6:89638712-89638761 | Rare:20 | ||||
| chr6:89829609-89829955 | Rare:89 |