| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10395090-10395242 | Rare:49 | ||||
| chr19:10502612-10503004 | Rare:105 | ||||
| chr19:10503293-10503381 | Rare:15 | ||||
| chr19:10565863-10566118 | Common:2; Rare:100 | ||||
| chr19:10568972-10569265 | Common:2; Rare:72 | ||||
| chr19:10653812-10653897 | Rare:32 | ||||
| chr19:10654686-10655046 | Common:6; Rare:150 | ||||
| chr19:10836194-10836558 | Common:2; Rare:97 | ||||
| chr19:10928556-10928795 | Common:1; Rare:66 | ||||
| chr19:10960689-10961106 | Common:3; Rare:162 | ||||
| chr19:11089295-11089516 | Rare:38; Clinvar:9; Clinvar (pathogenic):1 | ||||
| chr19:11155656-11156066 | Common:3; Rare:108 | ||||
| chr19:11197504-11197633 | Common:1; Rare:35 | ||||
| chr19:11197803-11197974 | Rare:55 | ||||
| chr19:11374919-11375236 | Common:1; Rare:82 |