| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128052170-128052525 | Common:2; Rare:120 | ||||
| chr3:128487892-128488078 | Common:1; Rare:49 | ||||
| chr3:128879423-128879694 | Common:4; Rare:135; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129183784-129184071 | Common:2; Rare:96 | ||||
| chr3:129249548-129249686 | Common:1; Rare:43 | ||||
| chr3:129278736-129278899 | Common:4; Rare:49 | ||||
| chr3:129316242-129316350 | Rare:50 | ||||
| chr3:129439838-129440350 | Common:1; Rare:157; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893545-129893887 | Rare:133 | ||||
| chr3:130893885-130894210 | Common:2; Rare:104 | ||||
| chr3:131026729-131026909 | Common:2; Rare:45 | ||||
| chr3:131381518-131381811 | Common:2; Rare:71 | ||||
| chr3:131502809-131503004 | Common:1; Rare:91 | ||||
| chr3:132417169-132417544 | Common:5; Rare:123 | ||||
| chr3:132659799-132659928 | Common:3; Rare:27 |