| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52278581-52278852 | Rare:101 | ||||
| chr3:52287702-52287857 | Common:2; Rare:56 | ||||
| chr3:52287998-52288168 | Rare:61 | ||||
| chr3:52409976-52410249 | Rare:68 | ||||
| chr3:52410810-52411447 | Common:4; Rare:178 | ||||
| chr3:52453915-52455150 | Common:12; Rare:277; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:52455455-52455642 | Common:2; Rare:65 | ||||
| chr3:52533133-52533234 | Common:1; Rare:21 | ||||
| chr3:52533806-52534016 | Common:2; Rare:64 | ||||
| chr3:52536360-52536697 | Common:2; Rare:107 | ||||
| chr3:52537020-52537290 | Rare:41 | ||||
| chr3:52685519-52685691 | Rare:54 | ||||
| chr3:52685933-52686051 | Common:1; Rare:43 | ||||
| chr3:52705694-52706181 | Common:3; Rare:165 | ||||
| chr3:52770908-52771121 | Common:3; Rare:70 |