| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:24495263-24495352 | Rare:32; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr6:24666601-24667317 | Common:4; Rare:285 | ||||
| chr6:24775194-24775471 | Common:2; Rare:73 | ||||
| chr6:25279210-25279529 | Common:2; Rare:115 | ||||
| chr6:26021382-26021653 | Common:2; Rare:73 | ||||
| chr6:26033616-26033792 | Common:2; Rare:40 | ||||
| chr6:26043709-26043952 | Common:3; Rare:85 | ||||
| chr6:26103711-26103993 | Common:5; Rare:122 | ||||
| chr6:26123905-26124192 | Common:5; Rare:125 | ||||
| chr6:26158101-26158286 | Common:1; Rare:116 | ||||
| chr6:26204461-26204666 | Common:1; Rare:111 | ||||
| chr6:26224026-26224236 | Common:5; Rare:43 | ||||
| chr6:26285501-26285719 | Common:5; Rare:106 | ||||
| chr6:26364912-26365231 | Common:4; Rare:64 | ||||
| chr6:26659703-26659882 | Rare:48 |