| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:55018309-55018848 | Common:8; Rare:203; Clinvar (benign):2 | ||||
| chr19:55038190-55038620 | Common:10; Rare:315 | ||||
| chr19:55041564-55042301 | Common:16; Rare:386 | ||||
| chr19:55042733-55043133 | Common:3; Rare:86 | ||||
| chr19:55043892-55044932 | Common:18; Rare:305 | ||||
| chr19:55062263-55062898 | Common:9; Rare:197 | ||||
| chr19:55063055-55063458 | Common:18; Rare:388 | ||||
| chr19:55069044-55069444 | Common:1; Rare:89 | ||||
| chr19:55071240-55071640 | Common:14; Rare:145 | ||||
| chr19:55080001-55080570 | Common:15; Rare:742 | ||||
| chr19:55080550-55081491 | Common:13; Rare:1135 | ||||
| chr19:55081421-55081786 | Rare:379 | ||||
| chr19:55115367-55115800 | Common:7; Rare:251 | ||||
| chr19:55117308-55117977 | Common:42; Rare:689 | ||||
| chr19:55136851-55137392 | Common:2; Rare:225; Clinvar:15; Clinvar (benign):2; Clinvar (pathogenic):2 |