| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:43465511-43465794 | Common:3; Rare:229 | ||||
| chr19:43504060-43504448 | Common:20; Rare:309 | ||||
| chr19:43504643-43504906 | Common:3; Rare:97 | ||||
| chr19:43527134-43527372 | Common:14; Rare:203; Clinvar:11; Clinvar (benign):20; Clinvar (pathogenic):6 | ||||
| chr19:43532596-43532768 | Common:2; Rare:33 | ||||
| chr19:43532740-43533010 | Common:1; Rare:51 | ||||
| chr19:43533000-43533627 | Common:9; Rare:379 | ||||
| chr19:43575410-43575855 | Common:9; Rare:328 | ||||
| chr19:43576241-43576570 | Common:3; Rare:186 | ||||
| chr19:43595965-43596693 | Common:14; Rare:579 | ||||
| chr19:43618965-43619145 | Rare:39 | ||||
| chr19:43619223-43619737 | Common:5; Rare:283 | ||||
| chr19:43619768-43620009 | Rare:113 | ||||
| chr19:43639771-43639979 | Common:3; Rare:177 | ||||
| chr19:43640130-43640380 | Common:1; Rare:35 |