| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46413515-46413739 | Common:1; Rare:74 | ||||
| chr19:46471412-46471640 | Common:8; Rare:81 | ||||
| chr19:46600847-46601437 | Common:6; Rare:198; Clinvar (benign):3 | ||||
| chr19:46608215-46608587 | Common:1; Rare:74; Clinvar (benign):7 | ||||
| chr19:46661330-46661529 | Rare:67 | ||||
| chr19:46697312-46697675 | Common:4; Rare:59 | ||||
| chr19:46746015-46746077 | Common:3; Rare:20 | ||||
| chr19:46746153-46746674 | Common:4; Rare:132 | ||||
| chr19:46838523-46838682 | Common:1; Rare:40 | ||||
| chr19:46850263-46850381 | Rare:18 | ||||
| chr19:47112124-47112393 | Rare:82 | ||||
| chr19:47112770-47112904 | Common:1; Rare:35 | ||||
| chr19:47113097-47113430 | Common:2; Rare:89 | ||||
| chr19:47113750-47113862 | Common:1; Rare:27 | ||||
| chr19:47130717-47130984 | Common:1; Rare:95 |