| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:51751846-51752092 | Common:2; Rare:57 | ||||
| chr19:52008130-52008359 | Rare:69 | ||||
| chr19:52048634-52048964 | Common:2; Rare:106 | ||||
| chr19:52269431-52269608 | Common:1; Rare:63 | ||||
| chr19:52397750-52397898 | Common:4; Rare:49 | ||||
| chr19:52735016-52735168 | Common:3; Rare:41 | ||||
| chr19:52786709-52786890 | Common:9; Rare:48 | ||||
| chr19:53333560-53333770 | Common:4; Rare:67 | ||||
| chr19:53538116-53538474 | Common:5; Rare:100 | ||||
| chr19:53554435-53554551 | Common:1; Rare:38 | ||||
| chr19:53867583-53867941 | Common:1; Rare:88 | ||||
| chr19:54102674-54102887 | Common:3; Rare:56 | ||||
| chr19:54115282-54115425 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr19:54115615-54115795 | Common:2; Rare:44; Clinvar:5 | ||||
| chr19:54159678-54160005 | Rare:117 |