| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:142596287-142596528 | Common:2; Rare:64 | ||||
| chr3:143001436-143001626 | Common:3; Rare:70 | ||||
| chr3:143971705-143971825 | Common:1; Rare:56 | ||||
| chr3:143971961-143972074 | Rare:43 | ||||
| chr3:146160942-146161285 | Common:1; Rare:117; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:146251010-146251196 | Common:1; Rare:48 | ||||
| chr3:146544467-146544792 | Common:4; Rare:80 | ||||
| chr3:149657977-149658159 | Rare:40 | ||||
| chr3:149813087-149813322 | Common:1; Rare:81 | ||||
| chr3:149970858-149970994 | Rare:74 | ||||
| chr3:150407984-150408314 | Common:2; Rare:96 | ||||
| chr3:150603151-150603365 | Common:2; Rare:85 | ||||
| chr3:150763146-150763270 | Rare:36 | ||||
| chr3:152268540-152269358 | Common:2; Rare:279 | ||||
| chr3:152269529-152269770 | Common:2; Rare:67 |