| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9621160-9621592 | Common:4; Rare:131 | ||||
| chr19:9768588-9768786 | Common:2; Rare:66 | ||||
| chr19:9786103-9786210 | Rare:30 | ||||
| chr19:9793161-9793239 | Rare:16 | ||||
| chr19:9818697-9818887 | Rare:81 | ||||
| chr19:9819054-9819141 | Rare:29 | ||||
| chr19:9827778-9827989 | Common:1; Rare:72 | ||||
| chr19:9834986-9835389 | Rare:159 | ||||
| chr19:9936350-9936635 | Common:4; Rare:99 | ||||
| chr19:10109675-10109970 | Common:1; Rare:107 | ||||
| chr19:10119838-10120038 | Common:1; Rare:74 | ||||
| chr19:10180556-10180839 | Common:2; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:10251777-10252032 | Common:1; Rare:62 | ||||
| chr19:10289563-10289787 | Common:2; Rare:51 | ||||
| chr19:10315858-10316050 | Common:4; Rare:98; Clinvar (benign):9 |