| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:8364022-8364172 | Common:1; Rare:39 | ||||
| chr19:8390032-8390456 | Common:2; Rare:118 | ||||
| chr19:8444720-8445061 | Common:4; Rare:150 | ||||
| chr19:8514138-8514222 | Common:1; Rare:27 | ||||
| chr19:9435475-9435641 | Common:1; Rare:63 | ||||
| chr19:9538574-9538748 | Common:1; Rare:53 | ||||
| chr19:9621167-9621525 | Common:4; Rare:103 | ||||
| chr19:9675033-9675143 | Rare:30 | ||||
| chr19:9768570-9768763 | Common:2; Rare:68 | ||||
| chr19:9818800-9818875 | Rare:29 | ||||
| chr19:9827833-9827982 | Common:1; Rare:55 | ||||
| chr19:9835012-9835396 | Rare:155 | ||||
| chr19:10270973-10271133 | Rare:44 | ||||
| chr19:10315851-10316262 | Common:4; Rare:147; Clinvar (benign):9 | ||||
| chr19:10333491-10333722 | Rare:83 |