| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38264358-38264676 | Common:3; Rare:81 | ||||
| chr19:38315755-38316088 | Rare:117 | ||||
| chr19:38336321-38336503 | Common:2; Rare:43 | ||||
| chr19:38337070-38337140 | Rare:16 | ||||
| chr19:38374406-38374836 | Rare:166 | ||||
| chr19:38618970-38619256 | Common:2; Rare:81 | ||||
| chr19:38647372-38647743 | Common:3; Rare:130 | ||||
| chr19:38831768-38832061 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr19:38852319-38852383 | Rare:16 | ||||
| chr19:38899528-38900026 | Rare:150 | ||||
| chr19:38930726-38930987 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39125558-39125808 | Rare:58 | ||||
| chr19:39391013-39391431 | Common:1; Rare:165 | ||||
| chr19:39406596-39406861 | Common:1; Rare:72 | ||||
| chr19:39435899-39436182 | Common:5; Rare:109 |