| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128487925-128488078 | Rare:37 | ||||
| chr3:128725983-128726197 | Common:1; Rare:60; Clinvar:2 | ||||
| chr3:128879404-128879698 | Common:4; Rare:146; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129161013-129161386 | Common:1; Rare:117 | ||||
| chr3:129183763-129184075 | Common:2; Rare:105 | ||||
| chr3:129249492-129249688 | Common:3; Rare:57 | ||||
| chr3:129278555-129278905 | Common:7; Rare:92 | ||||
| chr3:129316281-129316350 | Rare:24 | ||||
| chr3:129428604-129428745 | Rare:38 | ||||
| chr3:129439829-129440391 | Common:1; Rare:171; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:129893545-129893887 | Rare:133 | ||||
| chr3:130746775-130746913 | Common:3; Rare:47 | ||||
| chr3:130893919-130894259 | Common:3; Rare:99 | ||||
| chr3:131026720-131026955 | Common:2; Rare:59 | ||||
| chr3:131381451-131381811 | Common:3; Rare:91 |