| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:181711736-181711926 | Rare:68 | ||||
| chr3:182793395-182793713 | Common:3; Rare:84 | ||||
| chr3:182980487-182980809 | Common:3; Rare:109 | ||||
| chr3:183253019-183253288 | Common:3; Rare:81 | ||||
| chr3:183254037-183254117 | Common:1; Rare:21 | ||||
| chr3:183635491-183635753 | Common:4; Rare:73 | ||||
| chr3:183884813-183884969 | Rare:64 | ||||
| chr3:184017870-184018073 | Common:1; Rare:60 | ||||
| chr3:184134921-184135029 | Common:1; Rare:16 | ||||
| chr3:184135221-184135398 | Common:2; Rare:55; Clinvar:5 | ||||
| chr3:184155208-184155336 | Rare:34 | ||||
| chr3:184181775-184181967 | Rare:47 | ||||
| chr3:184185856-184186233 | Common:5; Rare:145 | ||||
| chr3:184248864-184249010 | Rare:82; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:184249512-184249768 | Common:1; Rare:78 |