| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41298419-41298612 | Rare:34 | ||||
| chr19:41310140-41310291 | Rare:67 | ||||
| chr19:41363794-41363983 | Common:1; Rare:69; Clinvar:1 | ||||
| chr19:41364136-41364453 | Rare:93 | ||||
| chr19:41439503-41439757 | Common:2; Rare:72 | ||||
| chr19:41549245-41549530 | Common:3; Rare:58 | ||||
| chr19:41688101-41688383 | Common:3; Rare:67 | ||||
| chr19:41708476-41708795 | Common:2; Rare:75 | ||||
| chr19:41710308-41710679 | Common:1; Rare:59 | ||||
| chr19:41755363-41755699 | Rare:74 | ||||
| chr19:41860126-41860289 | Common:1; Rare:65; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41883130-41883289 | Common:1; Rare:32 | ||||
| chr19:41884122-41884493 | Rare:103 | ||||
| chr19:41898047-41898368 | Common:1; Rare:77 | ||||
| chr19:41957046-41957376 | Common:3; Rare:69 |