| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49451730-49451998 | Common:3; Rare:69 | ||||
| chr19:49487278-49487644 | Common:5; Rare:130 | ||||
| chr19:49513102-49513403 | Common:1; Rare:69 | ||||
| chr19:49527864-49528031 | Common:3; Rare:51 | ||||
| chr19:49580534-49580620 | Rare:28 | ||||
| chr19:49665771-49665975 | Common:2; Rare:98; Clinvar (pathogenic):1 | ||||
| chr19:49677219-49677293 | Common:1; Rare:38 | ||||
| chr19:49690980-49691151 | Common:2; Rare:40 | ||||
| chr19:49808816-49808986 | Rare:57 | ||||
| chr19:49813249-49813350 | Rare:43 | ||||
| chr19:49818212-49818312 | Common:3; Rare:36; Clinvar:1 | ||||
| chr19:49851075-49851120 | Rare:16 | ||||
| chr19:49877319-49877717 | Common:1; Rare:99 | ||||
| chr19:49929404-49929820 | Common:7; Rare:141 | ||||
| chr19:49929923-49930219 | Common:1; Rare:70 |