| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49665761-49666041 | Common:3; Rare:135; Clinvar (pathogenic):1 | ||||
| chr19:49851058-49851120 | Rare:24 | ||||
| chr19:49867222-49867391 | Common:2; Rare:55; Clinvar (benign):2 | ||||
| chr19:49877268-49877724 | Common:2; Rare:116 | ||||
| chr19:49878018-49878192 | Common:1; Rare:61 | ||||
| chr19:49929404-49929820 | Common:7; Rare:141 | ||||
| chr19:49929923-49930191 | Common:1; Rare:55 | ||||
| chr19:50333357-50333657 | Common:3; Rare:62 | ||||
| chr19:50476370-50476544 | Rare:80 | ||||
| chr19:50511142-50511389 | Common:1; Rare:85 | ||||
| chr19:50658168-50658497 | Common:1; Rare:60 | ||||
| chr19:50723205-50723377 | Common:2; Rare:42 | ||||
| chr19:50804572-50804911 | Common:8; Rare:106 | ||||
| chr19:50968742-50969064 | Common:2; Rare:69 | ||||
| chr19:51366274-51366537 | Common:5; Rare:79; Clinvar (benign):2 |