| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42302316-42302902 | Common:3; Rare:137 | ||||
| chr19:42313294-42313516 | Common:1; Rare:57 | ||||
| chr19:42325391-42325675 | Rare:74 | ||||
| chr19:43504089-43504350 | Common:6; Rare:84 | ||||
| chr19:43504747-43504922 | Common:1; Rare:50 | ||||
| chr19:43527182-43527303 | Common:4; Rare:49; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:43575427-43575852 | Common:3; Rare:115 | ||||
| chr19:43596006-43596433 | Common:3; Rare:133 | ||||
| chr19:43619565-43619720 | Common:2; Rare:48 | ||||
| chr19:43754901-43755107 | Common:3; Rare:71 | ||||
| chr19:43827192-43827435 | Common:3; Rare:49 | ||||
| chr19:43901733-43901945 | Common:3; Rare:46 | ||||
| chr19:43935231-43935360 | Common:2; Rare:35 | ||||
| chr19:43951048-43951281 | Common:2; Rare:62 | ||||
| chr19:44002794-44003013 | Common:4; Rare:58 |