| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14402388-14402606 | Common:1; Rare:63 | ||||
| chr3:14651486-14651788 | Rare:82 | ||||
| chr3:14947209-14947557 | Common:4; Rare:156 | ||||
| chr3:14948394-14948637 | Common:2; Rare:67 | ||||
| chr3:15065219-15065369 | Common:2; Rare:61 | ||||
| chr3:15206066-15206264 | Rare:76 | ||||
| chr3:15427459-15427629 | Common:1; Rare:61 | ||||
| chr3:15601479-15601804 | Common:4; Rare:136; Clinvar:1 | ||||
| chr3:15601807-15602019 | Common:2; Rare:105; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:15797137-15797362 | Common:6; Rare:48 | ||||
| chr3:15859787-15860099 | Common:4; Rare:95 | ||||
| chr3:16264874-16265243 | Common:2; Rare:122 | ||||
| chr3:17742507-17742831 | Common:3; Rare:114 | ||||
| chr3:19946956-19947450 | Common:7; Rare:184 | ||||
| chr3:20186161-20186370 | Common:1; Rare:58 |