| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:125645123-125645282 | Common:1; Rare:38 | ||||
| chr6:126643566-126643611 | Common:1; Rare:14 | ||||
| chr6:126873907-126874091 | Common:2; Rare:33 | ||||
| chr6:127428555-127428775 | Common:2; Rare:45 | ||||
| chr6:128929943-128930069 | Common:3; Rare:37 | ||||
| chr6:129505090-129505322 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr6:129552564-129552671 | Rare:20 | ||||
| chr6:130138466-130138658 | Rare:34 | ||||
| chr6:131129767-131129991 | Common:3; Rare:36 | ||||
| chr6:132131773-132131945 | Rare:32 | ||||
| chr6:132817023-132817121 | Common:1; Rare:36 | ||||
| chr6:133088004-133088153 | Rare:29 | ||||
| chr6:134475472-134475616 | Common:1; Rare:23 | ||||
| chr6:134476507-134476680 | Common:2; Rare:26 | ||||
| chr6:134478861-134478910 | Common:1; Rare:7 |