| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127266773-127266920 | Common:1; Rare:66 | ||||
| chr6:127343325-127343644 | Common:2; Rare:74 | ||||
| chr6:127518930-127519090 | Common:2; Rare:25 | ||||
| chr6:128520539-128520752 | Rare:76 | ||||
| chr6:131135612-131135760 | Common:2; Rare:44 | ||||
| chr6:131951349-131951527 | Common:1; Rare:40 | ||||
| chr6:132401516-132401584 | Rare:27 | ||||
| chr6:132814339-132814678 | Common:4; Rare:135 | ||||
| chr6:132814705-132814764 | Common:2; Rare:38 | ||||
| chr6:133240867-133240882 | Rare:2 | ||||
| chr6:134174735-134175059 | Common:1; Rare:166 | ||||
| chr6:134175680-134175947 | Common:2; Rare:62 | ||||
| chr6:135054711-135054990 | Common:6; Rare:88 | ||||
| chr6:135497583-135497851 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:135851967-135852049 | Rare:22 |