| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:47349081-47349352 | Rare:74 | ||||
| chr19:47484182-47484302 | Common:2; Rare:38 | ||||
| chr19:47778438-47778776 | Common:2; Rare:115 | ||||
| chr19:48170270-48170704 | Common:2; Rare:117 | ||||
| chr19:48321347-48321495 | Common:1; Rare:43 | ||||
| chr19:48325321-48325610 | Common:2; Rare:63 | ||||
| chr19:48445866-48446041 | Common:1; Rare:62 | ||||
| chr19:48619139-48619435 | Rare:96 | ||||
| chr19:48624159-48624414 | Common:1; Rare:71 | ||||
| chr19:48646027-48646058 | Rare:6 | ||||
| chr19:48872218-48872438 | Common:2; Rare:71 | ||||
| chr19:48899994-48900383 | Common:1; Rare:108 | ||||
| chr19:48964974-48965355 | Common:1; Rare:91; Clinvar (pathogenic):4 | ||||
| chr19:48965357-48965609 | Rare:80; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr19:48993241-48993508 | Common:2; Rare:122; Clinvar:3; Clinvar (benign):2 |