| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123585491-123585586 | Rare:17 | ||||
| chr3:123692370-123692461 | Rare:19 | ||||
| chr3:123949545-123949957 | Common:2; Rare:69 | ||||
| chr3:123958789-123959146 | Rare:57 | ||||
| chr3:124730376-124730621 | Common:3; Rare:103; Clinvar:5; Clinvar (benign):3 | ||||
| chr3:124886932-124887157 | Common:1; Rare:68 | ||||
| chr3:124887261-124887604 | Rare:108 | ||||
| chr3:124887607-124887879 | Common:4; Rare:80 | ||||
| chr3:125375106-125375383 | Rare:68 | ||||
| chr3:125520032-125520392 | Rare:115 | ||||
| chr3:125595417-125595785 | Common:2; Rare:104 | ||||
| chr3:126083986-126084208 | Common:2; Rare:69 | ||||
| chr3:126704084-126704394 | Common:2; Rare:112 | ||||
| chr3:127590713-127590911 | Common:2; Rare:43 | ||||
| chr3:127598209-127598468 | Common:3; Rare:78 |