| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129160991-129161152 | Common:1; Rare:63 | ||||
| chr3:129183774-129184091 | Common:2; Rare:109 | ||||
| chr3:129249518-129249680 | Common:2; Rare:52 | ||||
| chr3:129278725-129278908 | Common:4; Rare:56 | ||||
| chr3:129316283-129316322 | Rare:18 | ||||
| chr3:129428593-129428774 | Common:1; Rare:46 | ||||
| chr3:129439814-129440481 | Common:5; Rare:211; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129893277-129893492 | Common:4; Rare:60 | ||||
| chr3:129893523-129893887 | Rare:138 | ||||
| chr3:130345784-130345934 | Common:5; Rare:24 | ||||
| chr3:130746375-130746414 | Rare:10 | ||||
| chr3:130746758-130746934 | Common:3; Rare:54 | ||||
| chr3:130850049-130850319 | Rare:53 | ||||
| chr3:130893899-130894336 | Common:3; Rare:123 | ||||
| chr3:131026563-131026968 | Common:2; Rare:93 |