| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45405970-45406210 | Common:3; Rare:78 | ||||
| chr19:45406321-45406699 | Common:3; Rare:91 | ||||
| chr19:45423475-45423959 | Common:7; Rare:154; Clinvar (benign):2 | ||||
| chr19:45423867-45423994 | Common:2; Rare:23 | ||||
| chr19:45424280-45424690 | Common:8; Rare:99 | ||||
| chr19:45469190-45469500 | Common:2; Rare:192 | ||||
| chr19:45493200-45493499 | Common:1; Rare:88; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:45496880-45497390 | Common:5; Rare:231 | ||||
| chr19:45506289-45506707 | Common:6; Rare:150 | ||||
| chr19:45506690-45507150 | Common:2; Rare:199 | ||||
| chr19:45507340-45507571 | Rare:124 | ||||
| chr19:45691850-45692130 | Rare:160 | ||||
| chr19:45692319-45692766 | Common:4; Rare:200 | ||||
| chr19:45730860-45731104 | Common:2; Rare:93 | ||||
| chr19:45768251-45768472 | Rare:158; Clinvar (benign):1; Clinvar (pathogenic):2 |