| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127266779-127266920 | Common:1; Rare:60 | ||||
| chr6:127343337-127343627 | Common:2; Rare:66 | ||||
| chr6:128520477-128520791 | Common:3; Rare:103 | ||||
| chr6:131628172-131628461 | Common:2; Rare:75 | ||||
| chr6:131950769-131951145 | Rare:134 | ||||
| chr6:132401396-132401595 | Common:1; Rare:60 | ||||
| chr6:132814276-132814611 | Common:3; Rare:122 | ||||
| chr6:133240998-133241435 | Common:5; Rare:129 | ||||
| chr6:133889002-133889188 | Common:1; Rare:32 | ||||
| chr6:133952949-133953269 | Common:2; Rare:92 | ||||
| chr6:134174847-134175010 | Common:1; Rare:73 | ||||
| chr6:135497612-135497873 | Common:4; Rare:95; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289774-136290014 | Common:1; Rare:104 | ||||
| chr6:136550409-136550659 | Common:2; Rare:70 | ||||
| chr6:137219109-137219307 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):3 |