| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9827838-9827954 | Common:1; Rare:45 | ||||
| chr19:9835012-9835347 | Rare:137 | ||||
| chr19:10333512-10333701 | Rare:63 | ||||
| chr19:10502708-10502926 | Rare:58 | ||||
| chr19:10928570-10928802 | Common:2; Rare:68 | ||||
| chr19:11089295-11089533 | Rare:44; Clinvar:10; Clinvar (pathogenic):1 | ||||
| chr19:11197504-11197622 | Common:1; Rare:32 | ||||
| chr19:11197837-11198006 | Rare:46 | ||||
| chr19:11374941-11375240 | Common:1; Rare:70 | ||||
| chr19:11559195-11559407 | Common:1; Rare:66 | ||||
| chr19:12551392-12551704 | Common:2; Rare:81 | ||||
| chr19:12610694-12610994 | Rare:98 | ||||
| chr19:12666697-12666809 | Rare:46; Clinvar:4 | ||||
| chr19:12722498-12722797 | Common:3; Rare:52 | ||||
| chr19:12734329-12734601 | Rare:68 |