| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39413625-39413676 | Rare:12 | ||||
| chr19:39435878-39436337 | Common:8; Rare:167 | ||||
| chr19:39445336-39445768 | Common:5; Rare:138 | ||||
| chr19:39480679-39481046 | Common:6; Rare:159; Clinvar (pathogenic):1 | ||||
| chr19:39481067-39481228 | Common:1; Rare:39 | ||||
| chr19:39532770-39533000 | Rare:93 | ||||
| chr19:39846294-39846632 | Common:1; Rare:131 | ||||
| chr19:39970553-39970682 | Common:1; Rare:17 | ||||
| chr19:39970705-39971241 | Common:8; Rare:141 | ||||
| chr19:39996460-39996545 | Common:1; Rare:15 | ||||
| chr19:39996867-39997237 | Common:5; Rare:83 | ||||
| chr19:39997269-39997375 | Rare:21 | ||||
| chr19:40056133-40056382 | Rare:39 | ||||
| chr19:40056405-40056540 | Common:1; Rare:29 | ||||
| chr19:40090405-40090505 | Common:1; Rare:24 |