| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142596262-142596459 | Common:2; Rare:52 | ||||
| chr3:142888823-142889304 | Common:4; Rare:110 | ||||
| chr3:143001454-143001654 | Common:2; Rare:75 | ||||
| chr3:143972014-143972081 | Common:1; Rare:24 | ||||
| chr3:146160899-146161388 | Common:2; Rare:153; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146222287-146222635 | Common:4; Rare:71 | ||||
| chr3:146250730-146251289 | Common:5; Rare:134 | ||||
| chr3:146544471-146544779 | Common:4; Rare:76 | ||||
| chr3:146544835-146544868 | Rare:9 | ||||
| chr3:148697767-148697902 | Rare:35; Clinvar:2 | ||||
| chr3:148991369-148991620 | Common:5; Rare:113; Clinvar (benign):1 | ||||
| chr3:149086490-149086699 | Rare:60 | ||||
| chr3:149129545-149129692 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377357-149377977 | Common:1; Rare:164 | ||||
| chr3:149657977-149658175 | Rare:43 |