| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45507314-45507499 | Rare:53 | ||||
| chr19:46601000-46601382 | Common:4; Rare:126 | ||||
| chr19:48170288-48170669 | Common:2; Rare:105 | ||||
| chr19:48619139-48619258 | Rare:53 | ||||
| chr19:49474126-49474270 | Common:1; Rare:33 | ||||
| chr19:49665777-49666020 | Common:2; Rare:124; Clinvar (pathogenic):1 | ||||
| chr19:52397683-52397879 | Common:3; Rare:56 | ||||
| chr19:54115288-54115402 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chr19:54115627-54115787 | Common:1; Rare:38; Clinvar:4 | ||||
| chr19:54449039-54449220 | Common:2; Rare:48 | ||||
| chr19:55370458-55370605 | Rare:25 | ||||
| chr19:55385759-55385961 | Common:5; Rare:67 | ||||
| chr19:56368112-56368330 | Common:2; Rare:74 | ||||
| chr19:56404025-56404357 | Common:5; Rare:95 | ||||
| chr19:57280433-57280503 | Rare:28 |