| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:127628970-127629220 | Common:1; Rare:83 | ||||
| chr3:127672830-127673007 | Common:1; Rare:86 | ||||
| chr3:128052147-128052500 | Common:3; Rare:116 | ||||
| chr3:128067279-128067547 | Rare:68 | ||||
| chr3:128879421-128879694 | Common:4; Rare:136; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129183784-129184071 | Common:2; Rare:96 | ||||
| chr3:129249498-129249714 | Common:3; Rare:65 | ||||
| chr3:129316278-129316338 | Rare:25 | ||||
| chr3:129439847-129440345 | Common:1; Rare:154; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129561290-129561419 | Common:1; Rare:35 | ||||
| chr3:129893535-129893866 | Rare:132 | ||||
| chr3:130746766-130746934 | Common:3; Rare:52 | ||||
| chr3:131026734-131026900 | Common:2; Rare:42 | ||||
| chr3:131381464-131381832 | Common:2; Rare:101 | ||||
| chr3:131502823-131502995 | Common:1; Rare:81 |