| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49085125-49085492 | Common:3; Rare:147 | ||||
| chr19:49453024-49453311 | Common:2; Rare:88 | ||||
| chr19:49580515-49580686 | Rare:58 | ||||
| chr19:49665765-49666034 | Common:2; Rare:133; Clinvar (pathogenic):1 | ||||
| chr19:49867527-49867643 | Common:2; Rare:38; Clinvar:1 | ||||
| chr19:49877319-49877541 | Rare:48 | ||||
| chr19:49929922-49930219 | Common:1; Rare:71 | ||||
| chr19:50384299-50384381 | Rare:33; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50476389-50476542 | Rare:73 | ||||
| chr19:50511144-50511383 | Common:1; Rare:83 | ||||
| chr19:50723223-50723406 | Common:2; Rare:42 | ||||
| chr19:50804926-50805119 | Common:2; Rare:55 | ||||
| chr19:51366333-51366544 | Common:5; Rare:55; Clinvar (benign):2 | ||||
| chr19:52008182-52008349 | Rare:46 | ||||
| chr19:52028344-52028460 | Common:3; Rare:23 |