| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:125956641-125956875 | Common:1; Rare:65 | ||||
| chr6:127266791-127266893 | Common:1; Rare:36 | ||||
| chr6:127343344-127343411 | Rare:9 | ||||
| chr6:128520553-128520798 | Common:1; Rare:89 | ||||
| chr6:129710088-129710322 | Rare:67 | ||||
| chr6:131951370-131951626 | Common:2; Rare:50 | ||||
| chr6:132814276-132814612 | Common:3; Rare:123 | ||||
| chr6:133953044-133953241 | Common:2; Rare:61 | ||||
| chr6:134174838-134175029 | Common:1; Rare:94 | ||||
| chr6:135054784-135054983 | Common:6; Rare:58 | ||||
| chr6:135497604-135497860 | Common:4; Rare:94; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136038337-136038422 | Rare:27 | ||||
| chr6:136289774-136290014 | Common:1; Rare:104 | ||||
| chr6:137219274-137219502 | Common:3; Rare:79; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:138404147-138404564 | Common:7; Rare:113 |