| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45424360-45424620 | Common:3; Rare:66 | ||||
| chr19:45450743-45451137 | Common:12; Rare:175 | ||||
| chr19:45469169-45469547 | Common:2; Rare:311 | ||||
| chr19:45469712-45469981 | Common:9; Rare:191 | ||||
| chr19:45478685-45479150 | Common:5; Rare:250 | ||||
| chr19:45493090-45493540 | Common:1; Rare:161; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr19:45496954-45497322 | Common:9; Rare:302 | ||||
| chr19:45499495-45500553 | Common:11; Rare:443 | ||||
| chr19:45506478-45506711 | Common:4; Rare:152 | ||||
| chr19:45506810-45507244 | Common:3; Rare:168 | ||||
| chr19:45507296-45507931 | Rare:315 | ||||
| chr19:45584204-45585127 | Common:18; Rare:655; Clinvar:11; Clinvar (benign):12 | ||||
| chr19:45616000-45616330 | Common:1; Rare:156 | ||||
| chr19:45637655-45638590 | Common:12; Rare:268 | ||||
| chr19:45639305-45639536 | Common:3; Rare:112 |