| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49362380-49362473 | Rare:26 | ||||
| chr19:49580540-49580644 | Rare:36 | ||||
| chr19:49665761-49666020 | Common:3; Rare:126; Clinvar (pathogenic):1 | ||||
| chr19:49877319-49877724 | Common:1; Rare:104 | ||||
| chr19:49929111-49929205 | Common:3; Rare:32 | ||||
| chr19:50476384-50476539 | Rare:71 | ||||
| chr19:50804590-50804913 | Common:6; Rare:97 | ||||
| chr19:51927418-51927509 | Common:1; Rare:26 | ||||
| chr19:52028336-52028420 | Common:2; Rare:22 | ||||
| chr19:52269397-52269615 | Common:1; Rare:84 | ||||
| chr19:52397738-52397879 | Common:2; Rare:41 | ||||
| chr19:52897674-52897874 | Rare:58 | ||||
| chr19:52962817-52963082 | Common:4; Rare:84 | ||||
| chr19:53254788-53255042 | Common:3; Rare:89 | ||||
| chr19:53467625-53467766 | Common:2; Rare:33 |