| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45730857-45731010 | Common:1; Rare:32 | ||||
| chr19:45769208-45769310 | Rare:27 | ||||
| chr19:46601194-46601434 | Common:4; Rare:71; Clinvar (benign):3 | ||||
| chr19:46788539-46788722 | Rare:46 | ||||
| chr19:47112151-47112329 | Rare:50 | ||||
| chr19:47778373-47778730 | Common:2; Rare:115 | ||||
| chr19:48170292-48170704 | Common:2; Rare:109 | ||||
| chr19:48445748-48446008 | Common:1; Rare:79 | ||||
| chr19:48551919-48552250 | Common:1; Rare:83 | ||||
| chr19:48619139-48619428 | Rare:92 | ||||
| chr19:48810988-48811086 | Rare:39 | ||||
| chr19:48964986-48965391 | Common:1; Rare:100; Clinvar (pathogenic):5 | ||||
| chr19:48965393-48965609 | Rare:66; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:48993266-48993516 | Common:2; Rare:111; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:49114084-49114401 | Common:4; Rare:79 |