| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120719595-120719798 | Rare:43 | ||||
| chr3:122074977-122075166 | Common:1; Rare:35 | ||||
| chr3:122430940-122431161 | Common:1; Rare:38 | ||||
| chr3:122726719-122726966 | Common:1; Rare:45 | ||||
| chr3:122727672-122727962 | Common:1; Rare:59 | ||||
| chr3:123618726-123619064 | Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:123626857-123627188 | Common:1; Rare:60; Clinvar:4; Clinvar (benign):3 | ||||
| chr3:123657677-123657723 | Common:1; Rare:8 | ||||
| chr3:124032896-124033073 | Rare:36 | ||||
| chr3:124156872-124157134 | Common:1; Rare:41 | ||||
| chr3:124699712-124700000 | Common:1; Rare:58 | ||||
| chr3:125594210-125594472 | Rare:42 | ||||
| chr3:125990557-125990581 | Rare:6 | ||||
| chr3:126448584-126448629 | Common:1; Rare:11 | ||||
| chr3:126989188-126989526 | Common:1; Rare:116 |