| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45886108-45886253 | Rare:87 | ||||
| chr19:45902586-45902919 | Common:6; Rare:194 | ||||
| chr19:46303507-46303620 | Common:1; Rare:14 | ||||
| chr19:46346909-46347146 | Common:6; Rare:143 | ||||
| chr19:46600888-46601402 | Common:10; Rare:327 | ||||
| chr19:46714270-46714500 | Common:3; Rare:81 | ||||
| chr19:46717074-46717227 | Common:2; Rare:48 | ||||
| chr19:46745903-46746088 | Common:3; Rare:44; Clinvar (benign):1 | ||||
| chr19:46746398-46746559 | Common:5; Rare:104 | ||||
| chr19:46784720-46785080 | Common:1; Rare:113 | ||||
| chr19:46787194-46787471 | Common:2; Rare:119 | ||||
| chr19:46788251-46788877 | Common:8; Rare:218 | ||||
| chr19:46850255-46850403 | Rare:43 | ||||
| chr19:47048541-47048912 | Common:2; Rare:231 | ||||
| chr19:47094240-47094830 | Common:1; Rare:222 |