| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41959260-41959485 | Common:1; Rare:73 | ||||
| chr19:42075794-42076199 | Common:4; Rare:115 | ||||
| chr19:42132409-42132627 | Rare:45 | ||||
| chr19:42220117-42220358 | Common:2; Rare:64 | ||||
| chr19:42268234-42268557 | Rare:65 | ||||
| chr19:42302436-42302478 | Rare:10 | ||||
| chr19:42302480-42302679 | Rare:55 | ||||
| chr19:42412395-42412713 | Common:2; Rare:56 | ||||
| chr19:42511947-42512177 | Rare:31 | ||||
| chr19:42528295-42528624 | Common:3; Rare:89; Clinvar:1 | ||||
| chr19:43525526-43525704 | Common:1; Rare:29 | ||||
| chr19:43525961-43526462 | Common:2; Rare:121; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:43527099-43527303 | Common:6; Rare:71; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr19:43595997-43596429 | Common:4; Rare:136 | ||||
| chr19:43668717-43669008 | Common:2; Rare:63 |