| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127343527-127343672 | Common:1; Rare:37 | ||||
| chr6:127459368-127459641 | Common:2; Rare:37 | ||||
| chr6:128520470-128520774 | Common:3; Rare:98 | ||||
| chr6:129710075-129710308 | Rare:71 | ||||
| chr6:130827415-130827439 | Rare:8 | ||||
| chr6:131573056-131573239 | Common:1; Rare:25; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:131628037-131628463 | Common:3; Rare:115 | ||||
| chr6:132401177-132401681 | Common:3; Rare:148 | ||||
| chr6:132402014-132402189 | Rare:36 | ||||
| chr6:133240736-133240883 | Rare:23 | ||||
| chr6:133888899-133889227 | Common:1; Rare:62 | ||||
| chr6:133889311-133889466 | Common:4; Rare:48; Clinvar:1 | ||||
| chr6:133889470-133889604 | Rare:48 | ||||
| chr6:133889633-133889766 | Common:1; Rare:23 | ||||
| chr6:133889770-133889846 | Common:1; Rare:17 |