| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19105662-19105866 | Common:1; Rare:69; Clinvar (pathogenic):1 | ||||
| chr19:19138374-19138638 | Common:3; Rare:80 | ||||
| chr19:19192038-19192346 | Common:4; Rare:90; Clinvar (benign):1 | ||||
| chr19:19192530-19192991 | Common:2; Rare:121 | ||||
| chr19:19203257-19203548 | Common:1; Rare:83 | ||||
| chr19:19320462-19320923 | Common:7; Rare:198 | ||||
| chr19:19321067-19321125 | Rare:16 | ||||
| chr19:19385224-19385374 | Rare:46 | ||||
| chr19:19385406-19385897 | Common:1; Rare:127 | ||||
| chr19:19386103-19386188 | Rare:18 | ||||
| chr19:19405471-19405889 | Common:4; Rare:141 | ||||
| chr19:19464468-19464682 | Common:2; Rare:35 | ||||
| chr19:19516056-19516357 | Rare:170; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19516419-19516535 | Common:1; Rare:37 | ||||
| chr19:19618626-19618919 | Common:1; Rare:91 |