| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9818809-9818887 | Rare:32 | ||||
| chr19:9827814-9827963 | Common:1; Rare:58 | ||||
| chr19:9835013-9835354 | Rare:138 | ||||
| chr19:10116951-10117152 | Rare:69 | ||||
| chr19:10119839-10120059 | Common:1; Rare:84 | ||||
| chr19:10315743-10316028 | Common:6; Rare:128; Clinvar (benign):10 | ||||
| chr19:10333484-10333709 | Common:1; Rare:78 | ||||
| chr19:10795941-10796182 | Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:10836268-10836561 | Common:2; Rare:77 | ||||
| chr19:10928551-10928724 | Common:1; Rare:46 | ||||
| chr19:11089274-11089499 | Rare:31; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:11197504-11197676 | Common:1; Rare:56 | ||||
| chr19:11374618-11374732 | Common:1; Rare:39 | ||||
| chr19:11374919-11375245 | Common:1; Rare:87 | ||||
| chr19:11418467-11418638 | Rare:36 |