| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:4061203-4061617 | Common:9; Rare:177 | ||||
| chr19:4061940-4062260 | Common:3; Rare:84 | ||||
| chr19:4063123-4063607 | Common:4; Rare:137 | ||||
| chr19:4064040-4064420 | Common:1; Rare:110 | ||||
| chr19:4064437-4064840 | Common:1; Rare:162 | ||||
| chr19:4067495-4067712 | Rare:61 | ||||
| chr19:4083970-4085144 | Common:10; Rare:507 | ||||
| chr19:4110225-4110901 | Common:8; Rare:262; Clinvar:10; Clinvar (benign):27; Clinvar (pathogenic):2 | ||||
| chr19:4375053-4375680 | Common:7; Rare:319 | ||||
| chr19:4375723-4376034 | Rare:106 | ||||
| chr19:4422640-4422950 | Rare:140 | ||||
| chr19:4493690-4494303 | Common:2; Rare:327 | ||||
| chr19:4792180-4793102 | Common:2; Rare:529 | ||||
| chr19:4800412-4800738 | Common:3; Rare:56 | ||||
| chr19:4800750-4801210 | Common:8; Rare:145 |