| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42132420-42132622 | Rare:40 | ||||
| chr19:42217658-42217933 | Common:1; Rare:104 | ||||
| chr19:42220112-42220358 | Common:2; Rare:66 | ||||
| chr19:42268262-42268570 | Rare:62 | ||||
| chr19:42302332-42302570 | Rare:70 | ||||
| chr19:42528424-42528580 | Common:2; Rare:38 | ||||
| chr19:43504066-43504393 | Common:7; Rare:105 | ||||
| chr19:43527173-43527303 | Common:4; Rare:55; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr19:43575465-43575760 | Common:1; Rare:89 | ||||
| chr19:43596073-43596433 | Common:2; Rare:111 | ||||
| chr19:43619570-43619646 | Rare:28 | ||||
| chr19:43754855-43755102 | Common:3; Rare:98 | ||||
| chr19:43780962-43781172 | Rare:43 | ||||
| chr19:43827186-43827433 | Common:2; Rare:49 | ||||
| chr19:43901782-43901917 | Common:2; Rare:29 |