| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:138348378-138348676 | Common:2; Rare:75 | ||||
| chr3:138594202-138594431 | Rare:65 | ||||
| chr3:138608722-138608883 | Rare:33 | ||||
| chr3:138608923-138609113 | Common:1; Rare:52 | ||||
| chr3:139344437-139344596 | Rare:25 | ||||
| chr3:139389568-139389876 | Common:2; Rare:98 | ||||
| chr3:139539449-139539835 | Common:3; Rare:122 | ||||
| chr3:140941632-140941907 | Common:2; Rare:106 | ||||
| chr3:141231616-141231888 | Common:2; Rare:94 | ||||
| chr3:141368396-141368540 | Rare:26 | ||||
| chr3:141486859-141487074 | Common:1; Rare:67 | ||||
| chr3:141876491-141876652 | Common:1; Rare:60 | ||||
| chr3:142225550-142225637 | Rare:29 | ||||
| chr3:142447890-142448185 | Common:1; Rare:94 | ||||
| chr3:142578702-142578976 | Rare:106; Clinvar:1; Clinvar (benign):1 |