| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:55166550-55166882 | Common:5; Rare:221; Clinvar:10; Clinvar (benign):8 | ||||
| chr19:55207133-55207384 | Common:2; Rare:146 | ||||
| chr19:55258340-55258776 | Common:7; Rare:251 | ||||
| chr19:55258946-55259233 | Common:2; Rare:208 | ||||
| chr19:55280187-55280600 | Common:1; Rare:153 | ||||
| chr19:55301760-55302190 | Common:11; Rare:188 | ||||
| chr19:55339561-55339958 | Common:2; Rare:208 | ||||
| chr19:55384183-55384635 | Common:6; Rare:137 | ||||
| chr19:55385375-55385535 | Common:4; Rare:70 | ||||
| chr19:55385704-55386007 | Common:12; Rare:193 | ||||
| chr19:55407584-55407879 | Common:6; Rare:241 | ||||
| chr19:55408000-55408400 | Common:2; Rare:202 | ||||
| chr19:55461530-55462004 | Common:12; Rare:245 | ||||
| chr19:55476140-55476360 | Common:2; Rare:90 | ||||
| chr19:55476440-55476650 | Common:4; Rare:137 |