| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:43754901-43755114 | Common:3; Rare:73 | ||||
| chr19:43780962-43781195 | Rare:49 | ||||
| chr19:43935231-43935405 | Common:3; Rare:50 | ||||
| chr19:44002823-44002963 | Common:2; Rare:33 | ||||
| chr19:44094214-44094410 | Common:1; Rare:45 | ||||
| chr19:44113242-44113451 | Common:2; Rare:41 | ||||
| chr19:44164981-44165133 | Common:1; Rare:37 | ||||
| chr19:44305001-44305141 | Rare:37 | ||||
| chr19:44500505-44500649 | Common:3; Rare:40 | ||||
| chr19:44955237-44955410 | Common:2; Rare:50 | ||||
| chr19:45038999-45039104 | Rare:41 | ||||
| chr19:45079130-45079319 | Common:1; Rare:49 | ||||
| chr19:45178626-45178788 | Common:4; Rare:37; Clinvar (benign):3 | ||||
| chr19:45370553-45370803 | Common:2; Rare:73 | ||||
| chr19:45406340-45406649 | Common:1; Rare:67 |