| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141231652-141231888 | Common:2; Rare:83 | ||||
| chr3:141323973-141324231 | Common:1; Rare:33 | ||||
| chr3:141402110-141402415 | Common:2; Rare:74 | ||||
| chr3:141876491-141876644 | Common:1; Rare:55 | ||||
| chr3:142578691-142578925 | Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:142962689-142962935 | Common:1; Rare:75 | ||||
| chr3:142963602-142963662 | Rare:19 | ||||
| chr3:143001454-143001646 | Common:2; Rare:70 | ||||
| chr3:146160896-146161387 | Common:2; Rare:153; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146222286-146222635 | Common:4; Rare:71 | ||||
| chr3:146544467-146544952 | Common:5; Rare:122 | ||||
| chr3:148697730-148697902 | Common:1; Rare:45; Clinvar:2 | ||||
| chr3:149129435-149129711 | Common:3; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377615-149377906 | Common:1; Rare:60 | ||||
| chr3:149474530-149475051 | Common:4; Rare:142 |