| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52403781-52404045 | Rare:74; Clinvar:15; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr3:52409976-52410245 | Rare:68 | ||||
| chr3:52454020-52454148 | Rare:34 | ||||
| chr3:52455429-52455732 | Common:2; Rare:100 | ||||
| chr3:52536640-52536758 | Common:1; Rare:45 | ||||
| chr3:52685593-52685809 | Common:2; Rare:52 | ||||
| chr3:52685912-52686179 | Common:2; Rare:103 | ||||
| chr3:52705576-52706267 | Common:4; Rare:227 | ||||
| chr3:52706418-52706689 | Common:1; Rare:73 | ||||
| chr3:52770894-52771120 | Common:4; Rare:78 | ||||
| chr3:53347493-53347741 | Common:2; Rare:81 | ||||
| chr3:53494126-53494220 | Common:3; Rare:31 | ||||
| chr3:53846412-53846585 | Rare:58 | ||||
| chr3:53891794-53892050 | Common:2; Rare:80 | ||||
| chr3:56557081-56557226 | Common:2; Rare:54 |