| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:54115271-54115441 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr19:54115628-54115792 | Common:1; Rare:40; Clinvar:4 | ||||
| chr19:54200685-54200891 | Common:2; Rare:78 | ||||
| chr19:54449028-54449229 | Common:2; Rare:57 | ||||
| chr19:55280084-55280157 | Rare:13 | ||||
| chr19:55385717-55385979 | Common:6; Rare:90 | ||||
| chr19:55461582-55461979 | Common:5; Rare:111 | ||||
| chr19:55654851-55655082 | Rare:86 | ||||
| chr19:56314815-56314933 | Common:1; Rare:35 | ||||
| chr19:56368259-56368360 | Common:2; Rare:34 | ||||
| chr19:56478060-56478249 | Common:2; Rare:65 | ||||
| chr19:56507562-56507863 | Common:3; Rare:78 | ||||
| chr19:56567371-56567681 | Common:2; Rare:79 | ||||
| chr19:56840690-56840880 | Common:1; Rare:53 | ||||
| chr19:57279865-57279995 | Rare:33 |