| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45079173-45079322 | Rare:39 | ||||
| chr19:45370548-45370799 | Common:2; Rare:74 | ||||
| chr19:45405024-45405224 | Common:1; Rare:43 | ||||
| chr19:45406350-45406687 | Common:2; Rare:85 | ||||
| chr19:45423480-45423779 | Common:2; Rare:58; Clinvar (benign):1 | ||||
| chr19:45423837-45423992 | Common:2; Rare:34 | ||||
| chr19:45424325-45424608 | Common:4; Rare:41 | ||||
| chr19:45496969-45497263 | Common:2; Rare:92 | ||||
| chr19:45507228-45507516 | Common:1; Rare:74 | ||||
| chr19:45692361-45692732 | Common:2; Rare:90 | ||||
| chr19:45730868-45731099 | Common:1; Rare:53 | ||||
| chr19:45863119-45863367 | Common:3; Rare:80 | ||||
| chr19:46346941-46347148 | Common:3; Rare:73 | ||||
| chr19:46600984-46601409 | Common:4; Rare:147; Clinvar (benign):1 | ||||
| chr19:46608290-46608487 | Common:1; Rare:53; Clinvar (benign):4 |