| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44500512-44500649 | Common:3; Rare:39 | ||||
| chr19:45406335-45406649 | Common:1; Rare:68 | ||||
| chr19:45450733-45451001 | Common:4; Rare:52 | ||||
| chr19:45507228-45507521 | Common:1; Rare:78 | ||||
| chr19:45692378-45692690 | Common:1; Rare:69 | ||||
| chr19:45730857-45730997 | Common:1; Rare:28 | ||||
| chr19:45769192-45769353 | Rare:54 | ||||
| chr19:46023034-46023212 | Common:3; Rare:43 | ||||
| chr19:46298357-46298473 | Rare:41 | ||||
| chr19:46346938-46347143 | Common:3; Rare:69 | ||||
| chr19:46413515-46413767 | Common:1; Rare:83 | ||||
| chr19:46600913-46601002 | Common:1; Rare:31 | ||||
| chr19:46601200-46601416 | Common:3; Rare:65; Clinvar (benign):1 | ||||
| chr19:46745847-46746066 | Common:3; Rare:44 | ||||
| chr19:46788573-46788677 | Rare:27 |