| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10795877-10796010 | Rare:34 | ||||
| chr19:10808195-10808406 | Rare:40 | ||||
| chr19:10836191-10836570 | Common:2; Rare:102 | ||||
| chr19:10928379-10928845 | Common:3; Rare:134 | ||||
| chr19:10960686-10961167 | Common:3; Rare:177; Clinvar (benign):2 | ||||
| chr19:11089378-11089545 | Rare:40; Clinvar:8; Clinvar (pathogenic):1 | ||||
| chr19:11155754-11156086 | Common:3; Rare:88 | ||||
| chr19:11197483-11197633 | Common:1; Rare:38 | ||||
| chr19:11374882-11375233 | Common:1; Rare:111 | ||||
| chr19:11381196-11381464 | Common:2; Rare:88; Clinvar:1 | ||||
| chr19:11384240-11384456 | Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:11435110-11435288 | Common:2; Rare:46 | ||||
| chr19:11449074-11449496 | Common:1; Rare:141; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr19:11505758-11506089 | Common:2; Rare:129 | ||||
| chr19:11538485-11538978 | Common:6; Rare:103 |