| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:680478-680760 | Common:2; Rare:97 | ||||
| chr19:821914-822067 | Rare:37 | ||||
| chr19:893158-893484 | Common:3; Rare:139 | ||||
| chr19:913173-913289 | Rare:34 | ||||
| chr19:925462-925778 | Common:8; Rare:97 | ||||
| chr19:984220-984434 | Common:1; Rare:84 | ||||
| chr19:1021119-1021543 | Common:15; Rare:179 | ||||
| chr19:1026488-1026723 | Rare:87 | ||||
| chr19:1067099-1067182 | Common:1; Rare:25 | ||||
| chr19:1103773-1104119 | Common:6; Rare:147 | ||||
| chr19:1105166-1105411 | Common:1; Rare:98 | ||||
| chr19:1269148-1269398 | Common:2; Rare:97 | ||||
| chr19:1354786-1355011 | Common:3; Rare:98 | ||||
| chr19:1383433-1383523 | Common:1; Rare:42 | ||||
| chr19:1401468-1401633 | Common:1; Rare:42; Clinvar:1; Clinvar (benign):5 |