| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:124730356-124730474 | Common:3; Rare:66; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:125375129-125375425 | Rare:83 | ||||
| chr3:127598229-127598446 | Common:3; Rare:57 | ||||
| chr3:127822451-127822674 | Rare:48 | ||||
| chr3:128052194-128052473 | Common:2; Rare:90 | ||||
| chr3:128123767-128123961 | Rare:49 | ||||
| chr3:128493200-128493339 | Rare:46 | ||||
| chr3:128879408-128879685 | Common:4; Rare:136; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:129183778-129184075 | Common:2; Rare:101 | ||||
| chr3:129249503-129249737 | Common:3; Rare:64 | ||||
| chr3:129278784-129278898 | Common:3; Rare:32 | ||||
| chr3:129316255-129316344 | Rare:37 | ||||
| chr3:129439846-129440291 | Common:1; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893558-129893887 | Rare:132 | ||||
| chr3:130746791-130746913 | Common:3; Rare:38 |