| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46600987-46601409 | Common:4; Rare:144; Clinvar (benign):1 | ||||
| chr19:46745847-46746066 | Common:3; Rare:44 | ||||
| chr19:47112151-47112463 | Rare:94 | ||||
| chr19:47256449-47256594 | Rare:53 | ||||
| chr19:47349073-47349373 | Rare:85 | ||||
| chr19:48170259-48170699 | Common:2; Rare:120 | ||||
| chr19:48445888-48446060 | Common:1; Rare:66 | ||||
| chr19:48619139-48619441 | Common:1; Rare:96 | ||||
| chr19:48740558-48740623 | Rare:13 | ||||
| chr19:48955158-48955330 | Common:1; Rare:39 | ||||
| chr19:48993253-48993923 | Common:8; Rare:231; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:49085098-49085525 | Common:3; Rare:169 | ||||
| chr19:49453077-49453311 | Common:1; Rare:77 | ||||
| chr19:49453473-49453612 | Rare:39 | ||||
| chr19:49513339-49513403 | Rare:14 |