| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48170241-48170704 | Common:3; Rare:129 | ||||
| chr19:48255395-48255724 | Common:4; Rare:59 | ||||
| chr19:48390881-48390957 | Rare:8 | ||||
| chr19:48445652-48445853 | Common:4; Rare:72 | ||||
| chr19:48445886-48446056 | Common:1; Rare:66 | ||||
| chr19:48619139-48619435 | Rare:96 | ||||
| chr19:48624057-48624426 | Common:1; Rare:91 | ||||
| chr19:48807261-48807393 | Common:1; Rare:26 | ||||
| chr19:48811005-48811124 | Rare:41 | ||||
| chr19:48872090-48872449 | Common:3; Rare:103 | ||||
| chr19:48918713-48919128 | Common:3; Rare:131 | ||||
| chr19:48933588-48933696 | Common:3; Rare:29 | ||||
| chr19:48965240-48965926 | Common:1; Rare:236; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):8 | ||||
| chr19:48993280-48993579 | Common:3; Rare:130; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:48993740-48993923 | Common:4; Rare:56 |