| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45469159-45469490 | Common:2; Rare:195 | ||||
| chr19:45496940-45497330 | Common:6; Rare:206 | ||||
| chr19:45506760-45507080 | Common:2; Rare:132 | ||||
| chr19:45507314-45507561 | Rare:146 | ||||
| chr19:45584310-45584670 | Common:2; Rare:203; Clinvar:2 | ||||
| chr19:45584761-45585054 | Common:8; Rare:215; Clinvar:3; Clinvar (benign):8 | ||||
| chr19:45639194-45639500 | Common:2; Rare:117 | ||||
| chr19:45642584-45642796 | Common:1; Rare:42 | ||||
| chr19:45691889-45692200 | Rare:171 | ||||
| chr19:45692319-45692766 | Common:5; Rare:203 | ||||
| chr19:45730836-45731078 | Common:2; Rare:81 | ||||
| chr19:45768247-45768476 | Rare:188; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr19:45769186-45769384 | Rare:131 | ||||
| chr19:45863049-45863398 | Common:9; Rare:206 | ||||
| chr19:45885810-45886050 | Rare:78 |