| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128052218-128052509 | Common:2; Rare:101 | ||||
| chr3:128067711-128068018 | Common:2; Rare:65 | ||||
| chr3:128123603-128123647 | Rare:10 | ||||
| chr3:128153350-128153505 | Rare:43 | ||||
| chr3:128650571-128650687 | Rare:45 | ||||
| chr3:128879421-128879675 | Common:4; Rare:124; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161017-129161169 | Common:1; Rare:60 | ||||
| chr3:129183814-129184065 | Common:2; Rare:83 | ||||
| chr3:129249498-129249690 | Common:3; Rare:56 | ||||
| chr3:129278736-129278895 | Common:4; Rare:49 | ||||
| chr3:129316284-129316422 | Common:1; Rare:35 | ||||
| chr3:129439829-129440325 | Common:1; Rare:149; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:130746763-130746934 | Common:3; Rare:52 | ||||
| chr3:130893885-130894237 | Common:3; Rare:107 | ||||
| chr3:131026735-131026889 | Common:2; Rare:38 |