| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10333503-10333694 | Rare:64 | ||||
| chr19:10380503-10380798 | Common:11; Rare:83; Clinvar:5 | ||||
| chr19:10625360-10625626 | Common:3; Rare:71 | ||||
| chr19:10654969-10655046 | Rare:20 | ||||
| chr19:10928527-10928681 | Common:1; Rare:39 | ||||
| chr19:11089162-11089529 | Rare:59; Clinvar:10; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:11090334-11090574 | Common:2; Rare:63 | ||||
| chr19:11155729-11156068 | Common:3; Rare:88 | ||||
| chr19:11374935-11375236 | Common:1; Rare:74 | ||||
| chr19:11435466-11435677 | Common:4; Rare:77; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:11559195-11559396 | Common:1; Rare:61 | ||||
| chr19:11597301-11597506 | Common:1; Rare:59 | ||||
| chr19:11738894-11739252 | Common:4; Rare:95 | ||||
| chr19:12484783-12484903 | Rare:26 | ||||
| chr19:12551452-12551676 | Common:2; Rare:59 |