| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9675022-9675134 | Rare:28 | ||||
| chr19:9768578-9768814 | Common:3; Rare:83 | ||||
| chr19:9793169-9793269 | Rare:18 | ||||
| chr19:9818809-9818887 | Rare:32 | ||||
| chr19:9827808-9827963 | Common:1; Rare:62 | ||||
| chr19:9835013-9835363 | Rare:142 | ||||
| chr19:9936367-9936635 | Common:4; Rare:95 | ||||
| chr19:10315729-10316033 | Common:6; Rare:139; Clinvar (benign):10 | ||||
| chr19:10333517-10333701 | Rare:62 | ||||
| chr19:10380503-10380792 | Common:11; Rare:80; Clinvar:5 | ||||
| chr19:10403383-10403929 | Rare:178 | ||||
| chr19:10568956-10569084 | Common:2; Rare:39 | ||||
| chr19:10602302-10602527 | Rare:69 | ||||
| chr19:10653817-10653887 | Rare:29 | ||||
| chr19:10836200-10836251 | Rare:13 |