| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18571631-18571904 | Common:3; Rare:113 | ||||
| chr19:18683495-18683702 | Common:1; Rare:70 | ||||
| chr19:18919295-18919740 | Common:3; Rare:175 | ||||
| chr19:18940273-18940329 | Rare:15 | ||||
| chr19:18941224-18941553 | Common:4; Rare:83 | ||||
| chr19:19033446-19033653 | Common:2; Rare:70 | ||||
| chr19:19033796-19033902 | Common:1; Rare:28 | ||||
| chr19:19105720-19105823 | Common:1; Rare:34; Clinvar (pathogenic):1 | ||||
| chr19:19192089-19192269 | Common:1; Rare:58 | ||||
| chr19:19192559-19192968 | Common:2; Rare:109 | ||||
| chr19:19320480-19320852 | Common:4; Rare:134 | ||||
| chr19:19516145-19516327 | Rare:115; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19653851-19654129 | Common:1; Rare:87 | ||||
| chr19:19655148-19655337 | Rare:65 | ||||
| chr19:19668470-19668949 | Common:3; Rare:136 |