| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12162923-12163132 | Rare:62 | ||||
| chr19:12333709-12333814 | Rare:22 | ||||
| chr19:12365619-12365794 | Common:3; Rare:45 | ||||
| chr19:12484740-12484923 | Rare:45 | ||||
| chr19:12551400-12551726 | Common:2; Rare:87 | ||||
| chr19:12610672-12610997 | Rare:104 | ||||
| chr19:12666699-12666865 | Rare:66; Clinvar:3 | ||||
| chr19:12681758-12681964 | Common:2; Rare:104; Clinvar (pathogenic):1 | ||||
| chr19:12696606-12696697 | Rare:45 | ||||
| chr19:12722482-12722802 | Common:4; Rare:53 | ||||
| chr19:12723924-12724089 | Common:1; Rare:36 | ||||
| chr19:12778422-12778483 | Rare:11 | ||||
| chr19:12791334-12791494 | Rare:34 | ||||
| chr19:12792234-12792273 | Common:1; Rare:9 | ||||
| chr19:12792296-12792591 | Rare:77 |