| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:139539491-139539757 | Common:3; Rare:93 | ||||
| chr3:140941641-140941911 | Common:2; Rare:103 | ||||
| chr3:141231623-141231888 | Common:2; Rare:91 | ||||
| chr3:141368264-141368548 | Rare:59 | ||||
| chr3:141402050-141402431 | Common:2; Rare:91 | ||||
| chr3:142578711-142578858 | Rare:54; Clinvar:1 | ||||
| chr3:143001472-143001631 | Common:2; Rare:57 | ||||
| chr3:146160973-146161276 | Common:1; Rare:105; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146250961-146251248 | Common:2; Rare:68 | ||||
| chr3:146544467-146544952 | Common:5; Rare:122 | ||||
| chr3:149377511-149377821 | Common:1; Rare:83 | ||||
| chr3:149812595-149812745 | Common:1; Rare:42 | ||||
| chr3:149813117-149813291 | Common:1; Rare:62 | ||||
| chr3:150603134-150603522 | Common:3; Rare:146 | ||||
| chr3:150703900-150704025 | Rare:44 |