| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46716885-46717307 | Common:7; Rare:180 | ||||
| chr19:46730990-46731420 | Rare:209 | ||||
| chr19:46732910-46733346 | Common:4; Rare:195 | ||||
| chr19:46745804-46746098 | Common:9; Rare:169; Clinvar (benign):2 | ||||
| chr19:46746130-46746360 | Common:1; Rare:46 | ||||
| chr19:46746349-46746573 | Common:7; Rare:180 | ||||
| chr19:46784672-46785106 | Common:5; Rare:252 | ||||
| chr19:46787201-46787721 | Common:3; Rare:371 | ||||
| chr19:46788096-46788909 | Common:12; Rare:393 | ||||
| chr19:46840090-46840480 | Common:1; Rare:74 | ||||
| chr19:46850178-46850886 | Rare:233 | ||||
| chr19:47035405-47036168 | Common:1; Rare:280 | ||||
| chr19:47047820-47048206 | Common:8; Rare:198 | ||||
| chr19:47048547-47048947 | Common:1; Rare:130 | ||||
| chr19:47094110-47094730 | Common:4; Rare:277 |