| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10836258-10836551 | Common:2; Rare:72 | ||||
| chr19:10928599-10928751 | Common:1; Rare:34 | ||||
| chr19:11089295-11089546 | Rare:52; Clinvar:12; Clinvar (pathogenic):1 | ||||
| chr19:11339487-11339798 | Common:4; Rare:73 | ||||
| chr19:11374889-11375239 | Common:1; Rare:108 | ||||
| chr19:11381221-11381427 | Common:1; Rare:68 | ||||
| chr19:11559201-11559475 | Common:4; Rare:81 | ||||
| chr19:11578704-11579011 | Common:1; Rare:62 | ||||
| chr19:12551452-12551699 | Common:2; Rare:63 | ||||
| chr19:12610723-12610981 | Rare:89 | ||||
| chr19:12666662-12666814 | Rare:65; Clinvar:4 | ||||
| chr19:12696629-12696731 | Rare:46 | ||||
| chr19:12778110-12778294 | Rare:40 | ||||
| chr19:12778398-12778566 | Common:2; Rare:26 | ||||
| chr19:12792809-12793049 | Rare:69 |