| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:56321519-56321675 | Rare:31 | ||||
| chr3:57952309-57952557 | Rare:39 | ||||
| chr3:61560693-61560823 | Common:1; Rare:45 | ||||
| chr3:61560879-61561037 | Common:2; Rare:45 | ||||
| chr3:68931675-68931949 | Common:3; Rare:66 | ||||
| chr3:69738438-69738568 | Common:1; Rare:21 | ||||
| chr3:71064047-71064291 | Common:2; Rare:66 | ||||
| chr3:71244269-71244449 | Common:1; Rare:47 | ||||
| chr3:75435034-75435313 | Common:4; Rare:99 | ||||
| chr3:75641095-75641302 | Rare:36 | ||||
| chr3:75672561-75672746 | Rare:1 | ||||
| chr3:78186624-78186669 | Rare:11 | ||||
| chr3:80770318-80770641 | Common:7; Rare:75 | ||||
| chr3:81761188-81761382 | Common:2; Rare:77; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:81761471-81761627 | Common:6; Rare:60; Clinvar:1; Clinvar (benign):3 |