| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38264750-38264981 | Common:1; Rare:70 | ||||
| chr19:38315797-38316104 | Rare:101 | ||||
| chr19:38374389-38374836 | Rare:172 | ||||
| chr19:38618920-38619325 | Common:3; Rare:114 | ||||
| chr19:38647372-38647748 | Common:3; Rare:132 | ||||
| chr19:38831736-38832061 | Common:4; Rare:107; Clinvar (benign):1 | ||||
| chr19:38899534-38900033 | Rare:152 | ||||
| chr19:38930723-38931002 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975691-38975833 | Common:1; Rare:33 | ||||
| chr19:39125558-39125805 | Rare:56 | ||||
| chr19:39342367-39342535 | Common:2; Rare:58 | ||||
| chr19:39390850-39390932 | Rare:35 | ||||
| chr19:39390990-39391476 | Common:1; Rare:189 | ||||
| chr19:39406706-39406880 | Rare:70 | ||||
| chr19:39412265-39412648 | Common:2; Rare:155 |