| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42423940-42424116 | Rare:33 | ||||
| chr19:43527182-43527286 | Common:4; Rare:45; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:43575454-43575746 | Common:2; Rare:88 | ||||
| chr19:43580449-43580643 | Common:4; Rare:34 | ||||
| chr19:43670129-43670409 | Common:2; Rare:65 | ||||
| chr19:43754901-43755106 | Common:3; Rare:70 | ||||
| chr19:43901767-43901873 | Common:1; Rare:22 | ||||
| chr19:44002783-44003014 | Common:4; Rare:61 | ||||
| chr19:44025228-44025399 | Common:1; Rare:35 | ||||
| chr19:44071991-44072173 | Common:1; Rare:41 | ||||
| chr19:44113145-44113440 | Common:4; Rare:68 | ||||
| chr19:44141500-44141661 | Common:1; Rare:21 | ||||
| chr19:44305001-44305157 | Rare:40 | ||||
| chr19:44356666-44356851 | Common:1; Rare:39 | ||||
| chr19:44500490-44500649 | Common:3; Rare:47 |