| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141876491-141876652 | Common:1; Rare:60 | ||||
| chr3:141921790-141922060 | Rare:49 | ||||
| chr3:142447913-142448130 | Common:1; Rare:66 | ||||
| chr3:142578700-142578925 | Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:143001436-143001646 | Common:3; Rare:79 | ||||
| chr3:143119619-143119855 | Common:1; Rare:69 | ||||
| chr3:143971754-143971845 | Common:1; Rare:42 | ||||
| chr3:143971961-143972074 | Rare:43 | ||||
| chr3:146160975-146161386 | Common:2; Rare:125; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146250967-146251229 | Common:1; Rare:63 | ||||
| chr3:146544467-146544876 | Common:5; Rare:99 | ||||
| chr3:148991383-148991626 | Common:2; Rare:111; Clinvar (benign):1 | ||||
| chr3:149086478-149086742 | Rare:78 | ||||
| chr3:149129549-149129843 | Common:1; Rare:117; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:149188052-149188377 | Common:1; Rare:56; Clinvar:1 |