| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128052149-128052552 | Common:3; Rare:137 | ||||
| chr3:128153352-128153487 | Rare:35 | ||||
| chr3:128487879-128488249 | Common:1; Rare:91 | ||||
| chr3:128488351-128488640 | Common:1; Rare:59 | ||||
| chr3:128726103-128726356 | Common:3; Rare:78; Clinvar:4; Clinvar (benign):4 | ||||
| chr3:128879408-128879676 | Common:4; Rare:130; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129160991-129161170 | Common:1; Rare:70 | ||||
| chr3:129183327-129183380 | Rare:21 | ||||
| chr3:129183822-129184078 | Common:2; Rare:87 | ||||
| chr3:129249501-129249744 | Common:3; Rare:67 | ||||
| chr3:129316276-129316295 | Rare:12 | ||||
| chr3:129439739-129440353 | Common:1; Rare:188; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893538-129893891 | Rare:138 | ||||
| chr3:130746744-130746929 | Common:3; Rare:57 | ||||
| chr3:130893956-130894242 | Common:3; Rare:85 |