| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:47112166-47112611 | Common:2; Rare:153 | ||||
| chr19:47256460-47256568 | Rare:39 | ||||
| chr19:47484191-47484300 | Common:1; Rare:35 | ||||
| chr19:47745440-47745562 | Rare:59 | ||||
| chr19:47778400-47778559 | Common:2; Rare:40 | ||||
| chr19:47778567-47778792 | Common:1; Rare:94 | ||||
| chr19:48170270-48170709 | Common:2; Rare:118 | ||||
| chr19:48445651-48445835 | Common:4; Rare:67 | ||||
| chr19:48445914-48446180 | Common:1; Rare:111 | ||||
| chr19:48619139-48619435 | Rare:96 | ||||
| chr19:48624228-48624426 | Common:1; Rare:56 | ||||
| chr19:48872189-48872437 | Common:2; Rare:76 | ||||
| chr19:48900154-48900372 | Common:1; Rare:70 | ||||
| chr19:48933451-48933714 | Common:3; Rare:76 | ||||
| chr19:48965038-48965355 | Common:1; Rare:83; Clinvar (pathogenic):4 |