| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:53254795-53255011 | Common:2; Rare:75 | ||||
| chr19:53333560-53333778 | Common:4; Rare:72 | ||||
| chr19:53365522-53365736 | Common:6; Rare:57 | ||||
| chr19:53431729-53432013 | Common:6; Rare:84 | ||||
| chr19:53866309-53866395 | Common:2; Rare:18 | ||||
| chr19:54102671-54102887 | Common:3; Rare:56 | ||||
| chr19:54115266-54115425 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr19:54115628-54115797 | Common:1; Rare:43; Clinvar:4 | ||||
| chr19:54159679-54160005 | Rare:117 | ||||
| chr19:54200658-54200952 | Common:5; Rare:103 | ||||
| chr19:54449028-54449249 | Common:2; Rare:65 | ||||
| chr19:54947491-54947604 | Common:1; Rare:29; Clinvar:1 | ||||
| chr19:54966241-54966406 | Common:2; Rare:47 | ||||
| chr19:55081485-55081725 | Rare:78 | ||||
| chr19:55166571-55166651 | Rare:39; Clinvar:3; Clinvar (benign):4 |