| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49453094-49453316 | Common:1; Rare:70 | ||||
| chr19:49453465-49453612 | Rare:45 | ||||
| chr19:49464077-49464161 | Rare:43 | ||||
| chr19:49496145-49496496 | Common:1; Rare:127 | ||||
| chr19:49580532-49580687 | Rare:48 | ||||
| chr19:49581306-49581464 | Common:1; Rare:31 | ||||
| chr19:49665591-49665975 | Common:6; Rare:172; Clinvar (pathogenic):1 | ||||
| chr19:49766914-49767113 | Common:1; Rare:79 | ||||
| chr19:49851058-49851124 | Rare:26 | ||||
| chr19:49867519-49867687 | Common:3; Rare:47; Clinvar:1 | ||||
| chr19:49877255-49877736 | Common:2; Rare:122 | ||||
| chr19:49877882-49878179 | Common:3; Rare:96 | ||||
| chr19:49929117-49929239 | Common:3; Rare:41 | ||||
| chr19:49929430-49929820 | Common:7; Rare:132 | ||||
| chr19:50025335-50025724 | Common:7; Rare:126 |