| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:128520476-128520807 | Common:4; Rare:112 | ||||
| chr6:129710160-129710317 | Rare:40 | ||||
| chr6:131063135-131063418 | Rare:78 | ||||
| chr6:131628045-131628450 | Common:3; Rare:112 | ||||
| chr6:132513005-132513259 | Common:1; Rare:60 | ||||
| chr6:132814276-132814612 | Common:3; Rare:123 | ||||
| chr6:133240532-133240661 | Rare:24 | ||||
| chr6:133240773-133240891 | Rare:17 | ||||
| chr6:133240940-133241451 | Common:5; Rare:152 | ||||
| chr6:133241855-133242086 | Common:1; Rare:56 | ||||
| chr6:133952367-133952468 | Rare:18 | ||||
| chr6:133953015-133953337 | Common:2; Rare:95 | ||||
| chr6:135054784-135055007 | Common:6; Rare:65 | ||||
| chr6:135497586-135497945 | Common:4; Rare:135; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:136250190-136250543 | Common:3; Rare:103 |