| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58476270-58476484 | Rare:181 | ||||
| chr19:58499122-58499710 | Common:10; Rare:507; Clinvar:24; Clinvar (benign):6 | ||||
| chr19:58519490-58520166 | Rare:423 | ||||
| chr19:58520170-58520480 | Common:1; Rare:93 | ||||
| chr19:58543890-58544227 | Common:5; Rare:204 | ||||
| chr19:58544163-58544586 | Common:5; Rare:426 | ||||
| chr19:58544781-58545181 | Rare:210 | ||||
| chr19:58554646-58554830 | Rare:45 | ||||
| chr19:58554926-58555262 | Common:6; Rare:309 | ||||
| chr19:58558316-58558769 | Rare:303 | ||||
| chr19:58558722-58559250 | Common:8; Rare:427 | ||||
| chr19:58559438-58559781 | Common:3; Rare:69 | ||||
| chr19:58571311-58571948 | Common:5; Rare:226 | ||||
| chr19:58571851-58572696 | Common:5; Rare:279 | ||||
| chr19:58572706-58573148 | Common:2; Rare:140 |