| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35269540-35269970 | Common:5; Rare:264 | ||||
| chr19:35282283-35282531 | Common:1; Rare:53; Clinvar:1 | ||||
| chr19:35309200-35309840 | Common:13; Rare:281 | ||||
| chr19:35309908-35310308 | Rare:251; Clinvar:5; Clinvar (benign):2 | ||||
| chr19:35318637-35319490 | Common:18; Rare:315 | ||||
| chr19:35545176-35545728 | Common:23; Rare:527 | ||||
| chr19:35545862-35546781 | Common:9; Rare:488 | ||||
| chr19:35557601-35558200 | Common:10; Rare:335 | ||||
| chr19:35612440-35612848 | Common:6; Rare:250 | ||||
| chr19:35628660-35629200 | Common:30; Rare:810 | ||||
| chr19:35641489-35641889 | Common:2; Rare:75 | ||||
| chr19:35642446-35643252 | Common:11; Rare:405 | ||||
| chr19:35643270-35643650 | Common:1; Rare:174 | ||||
| chr19:35643730-35643908 | Common:2; Rare:49 | ||||
| chr19:35648022-35648441 | Common:6; Rare:448; Clinvar:6; Clinvar (benign):6 |