| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142889072-142889334 | Common:1; Rare:39 | ||||
| chr3:143001420-143001662 | Common:3; Rare:94 | ||||
| chr3:143027019-143027251 | Common:1; Rare:28 | ||||
| chr3:143971692-143971850 | Common:1; Rare:74 | ||||
| chr3:146160825-146161222 | Common:3; Rare:145; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146161286-146161456 | Common:2; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:146222303-146222563 | Common:3; Rare:48 | ||||
| chr3:146251070-146251277 | Common:1; Rare:52 | ||||
| chr3:149060643-149060793 | Rare:46 | ||||
| chr3:149129542-149129737 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149333214-149333657 | Common:4; Rare:104 | ||||
| chr3:149333661-149333807 | Rare:30 | ||||
| chr3:149375194-149375576 | Common:2; Rare:93 | ||||
| chr3:149377368-149377869 | Common:1; Rare:145 | ||||
| chr3:149657439-149657592 | Common:1; Rare:23 |