| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:124963532-124963697 | Rare:29 | ||||
| chr6:125749370-125749762 | Common:6; Rare:156 | ||||
| chr6:125780864-125780920 | Rare:12 | ||||
| chr6:125781024-125781201 | Rare:29 | ||||
| chr6:125986425-125986548 | Rare:47 | ||||
| chr6:127118968-127119044 | Rare:10 | ||||
| chr6:127119806-127119887 | Rare:24 | ||||
| chr6:127266814-127266920 | Common:1; Rare:41 | ||||
| chr6:127343337-127343645 | Common:2; Rare:70 | ||||
| chr6:128520468-128520763 | Common:2; Rare:97 | ||||
| chr6:128883228-128883354 | Rare:44; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr6:131628108-131628412 | Common:3; Rare:87 | ||||
| chr6:132401435-132401605 | Common:1; Rare:49 | ||||
| chr6:133888919-133889217 | Common:1; Rare:54 | ||||
| chr6:133889331-133889614 | Common:4; Rare:97; Clinvar:1 |