| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143971967-143972074 | Rare:42 | ||||
| chr3:146160975-146161386 | Common:2; Rare:125; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146222284-146222635 | Common:4; Rare:71 | ||||
| chr3:146251015-146251237 | Common:2; Rare:57 | ||||
| chr3:146544442-146544792 | Common:4; Rare:84 | ||||
| chr3:149129545-149129687 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377640-149377985 | Common:1; Rare:68 | ||||
| chr3:149474773-149475024 | Common:2; Rare:89 | ||||
| chr3:149657964-149658212 | Rare:55 | ||||
| chr3:150408159-150408302 | Common:1; Rare:57 | ||||
| chr3:150603145-150603365 | Common:2; Rare:85 | ||||
| chr3:150763488-150763610 | Rare:32 | ||||
| chr3:151384745-151384999 | Common:1; Rare:43 | ||||
| chr3:152243450-152243713 | Common:1; Rare:43 | ||||
| chr3:152268838-152269109 | Rare:98 |