| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128052173-128052509 | Common:2; Rare:114 | ||||
| chr3:128067225-128067581 | Rare:86 | ||||
| chr3:128153264-128153510 | Common:2; Rare:67 | ||||
| chr3:128487920-128488074 | Rare:40 | ||||
| chr3:128879425-128879669 | Common:4; Rare:120; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183781-129184075 | Common:2; Rare:99 | ||||
| chr3:129249503-129249683 | Common:3; Rare:53 | ||||
| chr3:129278761-129278882 | Common:4; Rare:40 | ||||
| chr3:129315865-129316133 | Common:2; Rare:73 | ||||
| chr3:129316282-129316328 | Rare:20 | ||||
| chr3:129439829-129440350 | Common:1; Rare:161; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129562916-129563096 | Common:3; Rare:56 | ||||
| chr3:129586214-129586567 | Common:2; Rare:99 | ||||
| chr3:129893545-129893882 | Rare:132 | ||||
| chr3:130746796-130746856 | Rare:20 |