| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42313000-42313610 | Common:5; Rare:128 | ||||
| chr19:42325348-42325702 | Rare:303 | ||||
| chr19:42325679-42326405 | Common:3; Rare:234 | ||||
| chr19:42424079-42424633 | Common:3; Rare:229 | ||||
| chr19:42528457-42528586 | Common:1; Rare:27 | ||||
| chr19:43463269-43463669 | Common:4; Rare:333 | ||||
| chr19:43463640-43464050 | Rare:302 | ||||
| chr19:43503891-43504537 | Common:37; Rare:657 | ||||
| chr19:43504554-43505017 | Common:4; Rare:188 | ||||
| chr19:43527064-43527464 | Common:21; Rare:302; Clinvar:12; Clinvar (benign):28; Clinvar (pathogenic):8 | ||||
| chr19:43532901-43533649 | Common:9; Rare:449 | ||||
| chr19:43533875-43534092 | Rare:44 | ||||
| chr19:43574780-43575180 | Rare:108 | ||||
| chr19:43575442-43575870 | Common:10; Rare:403 | ||||
| chr19:43580251-43580764 | Common:21; Rare:237 |