| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1205453-1205810 | Common:2; Rare:114 | ||||
| chr19:1206494-1206894 | Common:4; Rare:251; Clinvar:10; Clinvar (benign):10 | ||||
| chr19:1237093-1237493 | Common:5; Rare:145 | ||||
| chr19:1237983-1238179 | Common:1; Rare:57 | ||||
| chr19:1241586-1241813 | Rare:71 | ||||
| chr19:1248464-1248606 | Common:1; Rare:49 | ||||
| chr19:1248950-1249151 | Common:1; Rare:61 | ||||
| chr19:1249528-1249921 | Common:2; Rare:162 | ||||
| chr19:1250882-1251202 | Common:1; Rare:149 | ||||
| chr19:1266317-1266717 | Common:7; Rare:249 | ||||
| chr19:1269181-1269358 | Common:1; Rare:70 | ||||
| chr19:1275325-1275576 | Common:1; Rare:129 | ||||
| chr19:1275770-1276076 | Common:2; Rare:138 | ||||
| chr19:1285770-1286170 | Common:1; Rare:146 | ||||
| chr19:1354744-1355031 | Common:3; Rare:135 |