| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42326384-42326418 | Rare:6 | ||||
| chr19:42422512-42422773 | Rare:56 | ||||
| chr19:42422850-42423084 | Common:1; Rare:47 | ||||
| chr19:42423094-42423417 | Common:2; Rare:85 | ||||
| chr19:42423501-42423847 | Common:4; Rare:114 | ||||
| chr19:42423937-42424083 | Rare:27 | ||||
| chr19:42528423-42528676 | Common:2; Rare:56 | ||||
| chr19:43504056-43504601 | Common:7; Rare:143 | ||||
| chr19:43504711-43504874 | Common:1; Rare:38 | ||||
| chr19:43525651-43525692 | Rare:3 | ||||
| chr19:43527144-43527340 | Common:5; Rare:73; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43533084-43533267 | Common:2; Rare:59 | ||||
| chr19:43575406-43575718 | Common:2; Rare:94 | ||||
| chr19:43580412-43580549 | Common:4; Rare:24 | ||||
| chr19:43595200-43595389 | Common:1; Rare:63 |