| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:14651453-14651786 | Rare:90 | ||||
| chr3:14947227-14947583 | Common:4; Rare:160 | ||||
| chr3:15099128-15099297 | Rare:42 | ||||
| chr3:15206075-15206287 | Rare:86 | ||||
| chr3:15427495-15427629 | Rare:47 | ||||
| chr3:15601466-15601758 | Common:4; Rare:115 | ||||
| chr3:15859777-15860121 | Common:4; Rare:108 | ||||
| chr3:16264818-16265234 | Common:2; Rare:144 | ||||
| chr3:19947051-19947384 | Common:4; Rare:124 | ||||
| chr3:23916919-23917359 | Rare:146 | ||||
| chr3:25783374-25783622 | Common:2; Rare:88; Clinvar (benign):3 | ||||
| chr3:29280791-29281087 | Common:4; Rare:56 | ||||
| chr3:33798517-33798695 | Common:2; Rare:65 | ||||
| chr3:36993159-36993487 | Common:2; Rare:87; Clinvar:14; Clinvar (benign):6 | ||||
| chr3:37176078-37176397 | Common:1; Rare:89 |