| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38647372-38647854 | Common:3; Rare:159 | ||||
| chr19:38831753-38832061 | Common:4; Rare:93; Clinvar (benign):1 | ||||
| chr19:38899513-38900041 | Rare:160 | ||||
| chr19:38930737-38930992 | Common:3; Rare:69; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39390990-39391432 | Common:1; Rare:170 | ||||
| chr19:39406699-39406848 | Rare:54 | ||||
| chr19:39435854-39436154 | Common:6; Rare:107 | ||||
| chr19:39480716-39480931 | Common:3; Rare:114; Clinvar (pathogenic):1 | ||||
| chr19:39970964-39971202 | Common:2; Rare:63 | ||||
| chr19:40056159-40056243 | Rare:14 | ||||
| chr19:40285272-40285572 | Common:1; Rare:112 | ||||
| chr19:40348393-40348746 | Common:4; Rare:114 | ||||
| chr19:40377835-40378070 | Common:2; Rare:91; Clinvar (benign):1 | ||||
| chr19:40716880-40716977 | Rare:22 | ||||
| chr19:40750426-40750909 | Common:6; Rare:119 |