| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:47484182-47484310 | Common:2; Rare:40 | ||||
| chr19:48170270-48170669 | Common:2; Rare:111 | ||||
| chr19:48619139-48619435 | Rare:96 | ||||
| chr19:48811010-48811126 | Rare:42 | ||||
| chr19:48965363-48965916 | Common:1; Rare:194; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr19:48993237-48993575 | Common:3; Rare:150; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:49085116-49085515 | Common:3; Rare:165 | ||||
| chr19:49527848-49528033 | Common:3; Rare:59 | ||||
| chr19:49580515-49580624 | Rare:43 | ||||
| chr19:49665747-49666020 | Common:3; Rare:130; Clinvar (pathogenic):1 | ||||
| chr19:49877319-49877717 | Common:1; Rare:99 | ||||
| chr19:49877836-49878145 | Common:5; Rare:96 | ||||
| chr19:50025335-50025709 | Common:7; Rare:118 | ||||
| chr19:50476349-50476542 | Rare:88 | ||||
| chr19:50723185-50723377 | Common:2; Rare:48 |