| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79947260-79947296 | Rare:13 | ||||
| chr6:80004352-80004674 | Common:7; Rare:80 | ||||
| chr6:81752675-81752830 | Rare:82 | ||||
| chr6:82247683-82247962 | Common:1; Rare:92 | ||||
| chr6:82364245-82364292 | Common:1; Rare:10 | ||||
| chr6:83067563-83067758 | Common:1; Rare:59 | ||||
| chr6:83193222-83193407 | Common:3; Rare:67 | ||||
| chr6:85593714-85594003 | Common:1; Rare:95 | ||||
| chr6:85643817-85643881 | Rare:25 | ||||
| chr6:87152555-87152618 | Rare:12 | ||||
| chr6:87155240-87155723 | Rare:146 | ||||
| chr6:87472892-87473006 | Common:1; Rare:43; Clinvar (benign):4 | ||||
| chr6:87589955-87590190 | Common:3; Rare:109; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87701503-87701669 | Common:1; Rare:55 | ||||
| chr6:87702169-87702472 | Common:3; Rare:94 |