| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48391481-48391674 | Rare:57 | ||||
| chr19:48445866-48446025 | Rare:55 | ||||
| chr19:48613893-48614054 | Common:2; Rare:42 | ||||
| chr19:48614609-48614710 | Rare:29 | ||||
| chr19:48614782-48615148 | Common:1; Rare:123 | ||||
| chr19:48619139-48619543 | Common:1; Rare:134 | ||||
| chr19:48624050-48624426 | Common:1; Rare:92 | ||||
| chr19:48695794-48696049 | Common:1; Rare:58 | ||||
| chr19:48807030-48807381 | Common:1; Rare:90 | ||||
| chr19:48811003-48811126 | Rare:43 | ||||
| chr19:48872247-48872455 | Common:2; Rare:80 | ||||
| chr19:48900056-48900410 | Common:1; Rare:106 | ||||
| chr19:48954596-48954922 | Common:1; Rare:115 | ||||
| chr19:48965042-48965355 | Common:1; Rare:82; Clinvar (pathogenic):4 | ||||
| chr19:48965357-48965609 | Rare:80; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 |