| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120908420-120908729 | Common:2; Rare:66 | ||||
| chr3:121749131-121749324 | Rare:35 | ||||
| chr3:121749450-121749522 | Rare:13 | ||||
| chr3:121749631-121750011 | Common:1; Rare:87 | ||||
| chr3:121834956-121835263 | Common:3; Rare:103; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383172-122383332 | Common:1; Rare:49 | ||||
| chr3:122384054-122384281 | Common:3; Rare:81 | ||||
| chr3:122416037-122416229 | Common:1; Rare:63 | ||||
| chr3:122514794-122515029 | Common:3; Rare:64 | ||||
| chr3:122564169-122564462 | Common:4; Rare:81 | ||||
| chr3:122680513-122680970 | Rare:127 | ||||
| chr3:122681060-122681226 | Rare:48 | ||||
| chr3:122793676-122793920 | Common:4; Rare:72 | ||||
| chr3:122794928-122795064 | Rare:49 | ||||
| chr3:123201687-123202026 | Common:2; Rare:96 |