| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:180989618-180989838 | Rare:91; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181711677-181711996 | Rare:90 | ||||
| chr3:182980977-182981180 | Rare:38 | ||||
| chr3:183099437-183099742 | Common:2; Rare:100; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr3:183253039-183253306 | Common:3; Rare:77 | ||||
| chr3:183555649-183555770 | Rare:32 | ||||
| chr3:183635507-183635707 | Common:2; Rare:63 | ||||
| chr3:183697679-183697959 | Common:2; Rare:114 | ||||
| chr3:183884837-183884969 | Rare:53 | ||||
| chr3:184017870-184018103 | Common:1; Rare:72 | ||||
| chr3:184135221-184135457 | Common:2; Rare:82; Clinvar:6 | ||||
| chr3:184185898-184186229 | Common:4; Rare:124 | ||||
| chr3:184261460-184261656 | Rare:38 | ||||
| chr3:184298942-184299269 | Common:3; Rare:100 | ||||
| chr3:184314428-184314663 | Common:3; Rare:71 |