| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50476384-50476542 | Rare:73 | ||||
| chr19:51366339-51366562 | Common:5; Rare:59; Clinvar (benign):2 | ||||
| chr19:52008182-52008284 | Rare:32 | ||||
| chr19:52028350-52028454 | Common:2; Rare:19 | ||||
| chr19:52397755-52397907 | Common:4; Rare:50 | ||||
| chr19:53132876-53132922 | Common:2; Rare:13 | ||||
| chr19:54115289-54115419 | Common:1; Rare:27; Clinvar (benign):1 | ||||
| chr19:54115444-54115792 | Common:3; Rare:79; Clinvar:6; Clinvar (benign):1 | ||||
| chr19:54159682-54160005 | Rare:115 | ||||
| chr19:54449022-54449238 | Common:3; Rare:59 | ||||
| chr19:54449412-54449516 | Rare:34 | ||||
| chr19:55385759-55385962 | Common:5; Rare:68 | ||||
| chr19:56368261-56368354 | Common:2; Rare:31 | ||||
| chr19:56404025-56404351 | Common:5; Rare:94 | ||||
| chr19:56477828-56478166 | Common:4; Rare:99 |