| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48624050-48624414 | Common:1; Rare:88 | ||||
| chr19:48868221-48868695 | Common:1; Rare:89 | ||||
| chr19:48933568-48933684 | Common:3; Rare:31 | ||||
| chr19:48954643-48954925 | Common:1; Rare:101 | ||||
| chr19:48993234-48993585 | Common:4; Rare:153; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:49085128-49085492 | Common:3; Rare:145 | ||||
| chr19:49157453-49157780 | Common:2; Rare:87; Clinvar:1 | ||||
| chr19:49361487-49361790 | Rare:52 | ||||
| chr19:49362390-49362473 | Rare:25 | ||||
| chr19:49446334-49446607 | Common:3; Rare:84 | ||||
| chr19:49453080-49453311 | Common:1; Rare:75 | ||||
| chr19:49527890-49528066 | Common:2; Rare:49 | ||||
| chr19:49580527-49580653 | Rare:43 | ||||
| chr19:49639967-49640469 | Common:1; Rare:159; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:49665667-49666041 | Common:5; Rare:172; Clinvar (pathogenic):1 |