| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41549277-41549529 | Common:3; Rare:50 | ||||
| chr19:41860103-41860285 | Common:1; Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41877018-41877311 | Common:1; Rare:52 | ||||
| chr19:41884132-41884437 | Rare:73 | ||||
| chr19:41959261-41959459 | Common:1; Rare:65 | ||||
| chr19:42075765-42076193 | Common:5; Rare:124 | ||||
| chr19:42132402-42132660 | Rare:54 | ||||
| chr19:42217705-42217954 | Common:1; Rare:88 | ||||
| chr19:42283766-42284053 | Rare:104 | ||||
| chr19:42423543-42423753 | Common:4; Rare:74 | ||||
| chr19:43504095-43504387 | Common:7; Rare:90 | ||||
| chr19:43575502-43575728 | Common:1; Rare:66 | ||||
| chr19:43596309-43596644 | Rare:106 | ||||
| chr19:43619577-43619686 | Common:1; Rare:32 | ||||
| chr19:43754541-43754763 | Common:3; Rare:73 |