| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12293909-12294134 | Common:3; Rare:37 | ||||
| chr19:12332454-12332554 | Rare:12 | ||||
| chr19:12440067-12440402 | Common:8; Rare:65 | ||||
| chr19:12495269-12495632 | Common:3; Rare:82 | ||||
| chr19:12612954-12613062 | Rare:17 | ||||
| chr19:12613780-12614091 | Common:3; Rare:53 | ||||
| chr19:12665252-12665441 | Rare:49; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:12782314-12782443 | Rare:30 | ||||
| chr19:12782454-12783010 | Common:7; Rare:179 | ||||
| chr19:12783276-12783566 | Common:1; Rare:58 | ||||
| chr19:12784617-12784856 | Common:3; Rare:44 | ||||
| chr19:12788699-12788787 | Rare:20 | ||||
| chr19:12788898-12789338 | Common:5; Rare:91 | ||||
| chr19:12789789-12790419 | Common:2; Rare:139 | ||||
| chr19:12793437-12793925 | Common:4; Rare:116 |