| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:183252929-183253329 | Common:7; Rare:178 | ||||
| chr3:183295270-183295688 | Common:4; Rare:148 | ||||
| chr3:183428105-183428348 | Rare:66 | ||||
| chr3:183428507-183428840 | Common:5; Rare:210 | ||||
| chr3:183635452-183635757 | Common:8; Rare:150 | ||||
| chr3:183636430-183636870 | Common:5; Rare:214 | ||||
| chr3:183697649-183697918 | Common:6; Rare:322 | ||||
| chr3:183824898-183825345 | Common:6; Rare:203 | ||||
| chr3:183825329-183825746 | Common:6; Rare:208 | ||||
| chr3:183884130-183885073 | Common:14; Rare:549 | ||||
| chr3:184017350-184017608 | Common:2; Rare:100 | ||||
| chr3:184017736-184018155 | Common:5; Rare:311 | ||||
| chr3:184134351-184135022 | Common:1; Rare:204 | ||||
| chr3:184135145-184135532 | Common:6; Rare:255; Clinvar:17 | ||||
| chr3:184135450-184135840 | Rare:163; Clinvar:4; Clinvar (pathogenic):4 |