| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48170262-48170705 | Common:2; Rare:120 | ||||
| chr19:48390835-48391014 | Rare:21 | ||||
| chr19:48445959-48446014 | Rare:17 | ||||
| chr19:48619139-48619694 | Common:1; Rare:167 | ||||
| chr19:48993238-48993516 | Common:2; Rare:123; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:49362386-49362467 | Rare:19 | ||||
| chr19:49447563-49447857 | Rare:73 | ||||
| chr19:49453092-49453328 | Common:1; Rare:73 | ||||
| chr19:49580518-49580665 | Rare:52 | ||||
| chr19:49640065-49640525 | Common:1; Rare:138 | ||||
| chr19:49665597-49666034 | Common:6; Rare:202; Clinvar (pathogenic):1 | ||||
| chr19:49851068-49851185 | Common:1; Rare:46 | ||||
| chr19:49877255-49877724 | Common:2; Rare:117 | ||||
| chr19:49877837-49878203 | Common:4; Rare:117 | ||||
| chr19:49878294-49878540 | Rare:58 |