| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45424366-45424449 | Common:2; Rare:11 | ||||
| chr19:45450769-45451021 | Common:4; Rare:49 | ||||
| chr19:45469185-45469473 | Common:1; Rare:93 | ||||
| chr19:45506527-45506629 | Common:1; Rare:34 | ||||
| chr19:45507391-45507510 | Rare:34 | ||||
| chr19:45584768-45585041 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45692303-45692713 | Common:1; Rare:95 | ||||
| chr19:45692875-45693090 | Common:1; Rare:38 | ||||
| chr19:45730869-45731073 | Common:1; Rare:45 | ||||
| chr19:45769185-45769642 | Common:1; Rare:186 | ||||
| chr19:45863119-45863376 | Common:3; Rare:81 | ||||
| chr19:45902611-45902922 | Common:3; Rare:91 | ||||
| chr19:45995283-45995498 | Rare:81 | ||||
| chr19:46346935-46347176 | Common:3; Rare:85 | ||||
| chr19:46601186-46601409 | Common:3; Rare:67; Clinvar (benign):1 |