| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:36214937-36215141 | Rare:53 | ||||
| chr19:36418604-36418747 | Common:1; Rare:59 | ||||
| chr19:36573227-36573388 | Common:3; Rare:48 | ||||
| chr19:36687390-36687616 | Common:2; Rare:70 | ||||
| chr19:37210530-37210630 | Common:1; Rare:21 | ||||
| chr19:37317666-37317911 | Common:6; Rare:59 | ||||
| chr19:38930732-38930987 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39390868-39391421 | Common:1; Rare:205 | ||||
| chr19:39435899-39436176 | Common:5; Rare:106 | ||||
| chr19:39480729-39480912 | Common:3; Rare:101; Clinvar (pathogenic):1 | ||||
| chr19:39846341-39846495 | Common:1; Rare:69 | ||||
| chr19:39970969-39971226 | Common:2; Rare:71 | ||||
| chr19:40056157-40056262 | Rare:15 | ||||
| chr19:40348364-40348715 | Common:4; Rare:110 | ||||
| chr19:40751064-40751323 | Common:3; Rare:76 |