| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48624046-48624431 | Common:1; Rare:94 | ||||
| chr19:48810846-48811158 | Rare:93 | ||||
| chr19:48872221-48872421 | Common:2; Rare:59 | ||||
| chr19:48933485-48933696 | Common:3; Rare:54 | ||||
| chr19:48954839-48954922 | Rare:31 | ||||
| chr19:48955170-48955580 | Common:3; Rare:91 | ||||
| chr19:48965663-48965916 | Common:1; Rare:94; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr19:48993281-48993575 | Common:3; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:49085055-49085531 | Common:3; Rare:181 | ||||
| chr19:49128088-49128258 | Common:2; Rare:55 | ||||
| chr19:49155394-49155580 | Rare:35 | ||||
| chr19:49453094-49453300 | Common:1; Rare:65 | ||||
| chr19:49453447-49453641 | Common:1; Rare:66 | ||||
| chr19:49513312-49513426 | Rare:24 | ||||
| chr19:49527775-49528032 | Common:4; Rare:81 |