| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45509348-45509415 | Common:1; Rare:26 | ||||
| chr19:45717264-45717526 | Common:1; Rare:85 | ||||
| chr19:46404217-46404351 | Common:1; Rare:27 | ||||
| chr19:46860822-46861127 | Common:3; Rare:99 | ||||
| chr19:47277703-47277843 | Common:1; Rare:28 | ||||
| chr19:48812268-48812508 | Common:2; Rare:47 | ||||
| chr19:48873023-48873264 | Common:2; Rare:43 | ||||
| chr19:48966277-48966681 | Rare:134; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:49491486-49491785 | Common:1; Rare:95 | ||||
| chr19:50491101-50491344 | Common:3; Rare:45 | ||||
| chr19:50497132-50497423 | Common:1; Rare:55 | ||||
| chr19:50500064-50500101 | Common:1; Rare:6 | ||||
| chr19:50500714-50500948 | Common:1; Rare:49 | ||||
| chr19:50501857-50502066 | Common:2; Rare:33 | ||||
| chr19:51688327-51688446 | Common:1; Rare:16 |