| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48933511-48933696 | Common:3; Rare:49 | ||||
| chr19:48993253-48993584 | Common:3; Rare:145; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:49085123-49085541 | Common:3; Rare:169 | ||||
| chr19:49114089-49114396 | Common:4; Rare:76 | ||||
| chr19:49149644-49149944 | Rare:60 | ||||
| chr19:49155364-49155531 | Rare:29 | ||||
| chr19:49210371-49210690 | Common:1; Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:49361515-49361795 | Rare:50 | ||||
| chr19:49362375-49362478 | Rare:31 | ||||
| chr19:49451748-49452022 | Common:3; Rare:77 | ||||
| chr19:49453094-49453311 | Common:1; Rare:69 | ||||
| chr19:49487284-49487644 | Common:5; Rare:129 | ||||
| chr19:49513108-49513467 | Common:1; Rare:77 | ||||
| chr19:49513741-49513995 | Common:4; Rare:66 | ||||
| chr19:49580515-49580656 | Rare:50 |