| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143001302-143001626 | Common:5; Rare:98 | ||||
| chr3:143971716-143971825 | Common:1; Rare:48 | ||||
| chr3:146160977-146161386 | Common:2; Rare:124; Clinvar:5; Clinvar (benign):2 | ||||
| chr3:146222296-146222635 | Common:4; Rare:68 | ||||
| chr3:146251000-146251360 | Common:2; Rare:90 | ||||
| chr3:146544467-146544920 | Common:5; Rare:115 | ||||
| chr3:149129549-149129697 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149377610-149377850 | Common:1; Rare:59 | ||||
| chr3:149378038-149378160 | Rare:21 | ||||
| chr3:149657952-149658306 | Rare:84 | ||||
| chr3:149813066-149813285 | Common:1; Rare:75 | ||||
| chr3:150407981-150408667 | Common:3; Rare:205 | ||||
| chr3:150410461-150410679 | Common:1; Rare:85 | ||||
| chr3:150603140-150603372 | Common:2; Rare:88 | ||||
| chr3:150703450-150703519 | Rare:20 |