| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49150329-49150692 | Rare:82 | ||||
| chr19:49157655-49157883 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:49210711-49211103 | Rare:136; Clinvar:6; Clinvar (benign):7 | ||||
| chr19:49361449-49361903 | Common:3; Rare:89 | ||||
| chr19:49362042-49362143 | Common:1; Rare:16 | ||||
| chr19:49362145-49362657 | Common:3; Rare:102 | ||||
| chr19:49362804-49363123 | Common:17; Rare:66 | ||||
| chr19:49363377-49363851 | Common:10; Rare:119 | ||||
| chr19:49441501-49441649 | Common:2; Rare:31 | ||||
| chr19:49451337-49451503 | Common:1; Rare:49 | ||||
| chr19:49451665-49452055 | Common:4; Rare:95 | ||||
| chr19:49452983-49453151 | Common:2; Rare:50 | ||||
| chr19:49453222-49453733 | Common:3; Rare:172 | ||||
| chr19:49474018-49474266 | Common:1; Rare:60 | ||||
| chr19:49478845-49479014 | Rare:48 |