| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38210682-38210904 | Common:1; Rare:43 | ||||
| chr19:38211029-38211866 | Common:4; Rare:262 | ||||
| chr19:38251352-38251758 | Common:2; Rare:158 | ||||
| chr19:38300761-38301161 | Common:3; Rare:117 | ||||
| chr19:38362286-38362686 | Common:2; Rare:157 | ||||
| chr19:38434610-38434970 | Common:2; Rare:63 | ||||
| chr19:38693448-38693848 | Common:4; Rare:89 | ||||
| chr19:38722128-38722278 | Common:2; Rare:43 | ||||
| chr19:39199074-39199474 | Common:4; Rare:154 | ||||
| chr19:39320109-39320905 | Common:4; Rare:199 | ||||
| chr19:39402161-39402561 | Common:2; Rare:93 | ||||
| chr19:39402551-39403004 | Rare:184 | ||||
| chr19:39403726-39403910 | Rare:32 | ||||
| chr19:39497942-39498167 | Common:2; Rare:57 | ||||
| chr19:39507118-39507436 | Rare:144; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 |