| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49084850-49085542 | Common:3; Rare:220 | ||||
| chr19:49085626-49085697 | Rare:33 | ||||
| chr19:49085778-49085889 | Common:1; Rare:28 | ||||
| chr19:49114234-49114434 | Common:2; Rare:56 | ||||
| chr19:49118675-49118880 | Common:2; Rare:83 | ||||
| chr19:49118955-49119192 | Rare:81 | ||||
| chr19:49127898-49128312 | Common:2; Rare:104 | ||||
| chr19:49142989-49143190 | Common:4; Rare:50 | ||||
| chr19:49149198-49149587 | Common:1; Rare:142 | ||||
| chr19:49149785-49149986 | Common:1; Rare:40 | ||||
| chr19:49150222-49150736 | Rare:113 | ||||
| chr19:49157632-49157908 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:49158236-49158362 | Common:2; Rare:47; Clinvar (benign):1 | ||||
| chr19:49361500-49361735 | Rare:39 | ||||
| chr19:49362372-49362467 | Rare:21 |