| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127343327-127343645 | Common:2; Rare:74 | ||||
| chr6:128520462-128520763 | Common:2; Rare:97 | ||||
| chr6:129710137-129710322 | Rare:49 | ||||
| chr6:131628107-131628477 | Common:3; Rare:96 | ||||
| chr6:131950768-131951216 | Rare:152 | ||||
| chr6:132401332-132401605 | Common:2; Rare:89 | ||||
| chr6:133889048-133889227 | Rare:29 | ||||
| chr6:133889359-133889604 | Common:2; Rare:83; Clinvar:1 | ||||
| chr6:133952379-133952482 | Rare:17 | ||||
| chr6:133953044-133953269 | Common:2; Rare:74 | ||||
| chr6:134174857-134175014 | Common:1; Rare:68 | ||||
| chr6:135054784-135054915 | Common:3; Rare:38 | ||||
| chr6:135497604-135497827 | Common:4; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289140-136289460 | Rare:112 | ||||
| chr6:136289756-136290063 | Common:2; Rare:136 |