| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18791296-18791389 | Rare:35 | ||||
| chr19:18919344-18919756 | Common:2; Rare:147 | ||||
| chr19:18924007-18924278 | Common:1; Rare:72 | ||||
| chr19:18940436-18940490 | Common:1; Rare:11 | ||||
| chr19:19033462-19033646 | Common:2; Rare:64 | ||||
| chr19:19033799-19033938 | Common:1; Rare:36 | ||||
| chr19:19192098-19192268 | Common:1; Rare:55 | ||||
| chr19:19320464-19320862 | Common:4; Rare:152 | ||||
| chr19:19321885-19321936 | Rare:10 | ||||
| chr19:19385904-19386067 | Rare:64 | ||||
| chr19:19516157-19516331 | Rare:103; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19628169-19628293 | Rare:31 | ||||
| chr19:19821131-19821339 | Common:2; Rare:37 | ||||
| chr19:29212925-29213233 | Common:3; Rare:85 | ||||
| chr19:29606163-29606317 | Rare:50 |