| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143119666-143119914 | Common:1; Rare:79 | ||||
| chr3:146160973-146161386 | Common:2; Rare:127; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146251006-146251221 | Common:1; Rare:54 | ||||
| chr3:146544490-146544919 | Common:4; Rare:108 | ||||
| chr3:149129545-149129676 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:149377494-149377841 | Common:1; Rare:95 | ||||
| chr3:149657971-149658295 | Rare:81 | ||||
| chr3:149813009-149813265 | Common:2; Rare:86 | ||||
| chr3:150603149-150603365 | Common:2; Rare:85 | ||||
| chr3:150703900-150704039 | Rare:46 | ||||
| chr3:152268585-152269169 | Common:2; Rare:210 | ||||
| chr3:152269226-152269339 | Rare:35 | ||||
| chr3:152269529-152269759 | Common:2; Rare:67 | ||||
| chr3:152269847-152270054 | Common:4; Rare:53 | ||||
| chr3:152298961-152299221 | Common:1; Rare:56 |