| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:124730387-124730468 | Common:2; Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:125375236-125375426 | Rare:57 | ||||
| chr3:125520162-125520297 | Rare:39 | ||||
| chr3:125595252-125595359 | Common:2; Rare:38 | ||||
| chr3:125595538-125595675 | Rare:45 | ||||
| chr3:126084103-126084422 | Common:2; Rare:105 | ||||
| chr3:127598220-127598443 | Common:3; Rare:58 | ||||
| chr3:127628970-127629211 | Common:1; Rare:79 | ||||
| chr3:128052170-128052500 | Common:2; Rare:110 | ||||
| chr3:128153356-128153531 | Rare:54 | ||||
| chr3:128487914-128488094 | Common:1; Rare:48 | ||||
| chr3:128725960-128726202 | Common:1; Rare:66; Clinvar:2 | ||||
| chr3:128879440-128879694 | Common:4; Rare:130; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129160991-129161150 | Common:1; Rare:63 | ||||
| chr3:129183774-129184084 | Common:2; Rare:105 |