| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19033446-19033799 | Common:2; Rare:105 | ||||
| chr19:19033805-19033933 | Common:1; Rare:35 | ||||
| chr19:19105685-19105879 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
| chr19:19170205-19170418 | Common:2; Rare:52 | ||||
| chr19:19192092-19192269 | Common:1; Rare:57 | ||||
| chr19:19192593-19193030 | Common:3; Rare:103; Clinvar (benign):1 | ||||
| chr19:19261594-19261964 | Common:3; Rare:102 | ||||
| chr19:19320472-19320862 | Common:4; Rare:146 | ||||
| chr19:19405563-19405827 | Common:4; Rare:94 | ||||
| chr19:19516136-19516328 | Rare:123; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19628427-19628661 | Rare:45 | ||||
| chr19:19643530-19643736 | Common:3; Rare:69 | ||||
| chr19:19663296-19663336 | Rare:14 | ||||
| chr19:19663640-19663749 | Rare:26 | ||||
| chr19:19664037-19664185 | Common:1; Rare:41 |