| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:122789491-122789810 | Common:1; Rare:82 | ||||
| chr6:124963016-124963336 | Common:2; Rare:108 | ||||
| chr6:125153701-125153968 | Rare:63 | ||||
| chr6:125301870-125302434 | Common:9; Rare:135 | ||||
| chr6:125749413-125749682 | Common:5; Rare:112 | ||||
| chr6:125781060-125781182 | Rare:21 | ||||
| chr6:125790858-125791034 | Common:2; Rare:54 | ||||
| chr6:125986382-125986690 | Rare:117 | ||||
| chr6:127266714-127266925 | Common:2; Rare:100 | ||||
| chr6:127343337-127343645 | Common:2; Rare:70 | ||||
| chr6:128520561-128520781 | Common:1; Rare:80 | ||||
| chr6:131063142-131063374 | Rare:63 | ||||
| chr6:131572940-131573338 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr6:131628083-131628439 | Common:3; Rare:95 | ||||
| chr6:132401351-132401605 | Common:2; Rare:83 |