| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19192088-19192327 | Common:1; Rare:70 | ||||
| chr19:19192496-19192977 | Common:2; Rare:122 | ||||
| chr19:19193107-19193152 | Rare:7 | ||||
| chr19:19203283-19203540 | Common:1; Rare:71 | ||||
| chr19:19320391-19320971 | Common:8; Rare:243 | ||||
| chr19:19321047-19321125 | Rare:22 | ||||
| chr19:19385206-19386045 | Common:1; Rare:252 | ||||
| chr19:19386135-19386271 | Common:1; Rare:30 | ||||
| chr19:19405364-19405859 | Common:4; Rare:152 | ||||
| chr19:19515927-19516515 | Common:3; Rare:263; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19618644-19618961 | Rare:104 | ||||
| chr19:19628127-19628391 | Rare:70 | ||||
| chr19:19643136-19643341 | Common:1; Rare:42 | ||||
| chr19:19643522-19643774 | Common:3; Rare:84 | ||||
| chr19:19661898-19662061 | Common:2; Rare:41 |