| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:183825561-183825841 | Common:2; Rare:66 | ||||
| chr3:183884812-183885037 | Rare:81 | ||||
| chr3:184017834-184018117 | Common:2; Rare:93 | ||||
| chr3:184135209-184135425 | Common:2; Rare:69; Clinvar:6 | ||||
| chr3:184155207-184155502 | Rare:84 | ||||
| chr3:184176604-184176918 | Common:3; Rare:60 | ||||
| chr3:184181686-184181999 | Rare:66 | ||||
| chr3:184185908-184186256 | Common:4; Rare:131 | ||||
| chr3:184187893-184188217 | Common:1; Rare:103 | ||||
| chr3:184243599-184243831 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:184248868-184249021 | Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249441-184249812 | Common:1; Rare:115 | ||||
| chr3:184298979-184299349 | Common:4; Rare:110 | ||||
| chr3:184305844-184306155 | Common:1; Rare:68 | ||||
| chr3:184306465-184306834 | Common:1; Rare:87 |