| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10105165-10105344 | Common:1; Rare:33 | ||||
| chr19:16283589-16283820 | Common:1; Rare:54 | ||||
| chr19:18905569-18905577 | Rare:1 | ||||
| chr19:19776391-19776596 | Common:2; Rare:55 | ||||
| chr19:23274194-23274360 | Common:2; Rare:44 | ||||
| chr19:23762848-23763037 | Common:2; Rare:65 | ||||
| chr19:27793376-27793477 | Common:1; Rare:28 | ||||
| chr19:27793667-27794039 | Rare:96 | ||||
| chr19:36151330-36151448 | Common:2; Rare:25 | ||||
| chr19:41500612-41500723 | Rare:17 | ||||
| chr19:42396940-42397184 | Rare:55 | ||||
| chr19:46404231-46404319 | Common:1; Rare:17 | ||||
| chr19:46412074-46412620 | Common:2; Rare:195; Clinvar (pathogenic):1 | ||||
| chr19:46860812-46861126 | Common:3; Rare:102 | ||||
| chr19:48912791-48913191 | Common:1; Rare:135 |