| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:43754890-43755102 | Common:3; Rare:80 | ||||
| chr19:43901798-43901894 | Common:2; Rare:20 | ||||
| chr19:43935231-43935360 | Common:2; Rare:35 | ||||
| chr19:44141472-44141620 | Common:2; Rare:20 | ||||
| chr19:44164981-44165142 | Common:1; Rare:40 | ||||
| chr19:44356651-44356851 | Common:1; Rare:41 | ||||
| chr19:44643822-44644040 | Rare:52 | ||||
| chr19:45038966-45039094 | Rare:42 | ||||
| chr19:45370544-45370731 | Common:2; Rare:57 | ||||
| chr19:45406355-45406694 | Common:3; Rare:86 | ||||
| chr19:45423466-45423702 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr19:45423837-45423992 | Common:2; Rare:34 | ||||
| chr19:45507228-45507516 | Common:1; Rare:74 | ||||
| chr19:45692365-45692738 | Common:2; Rare:93 | ||||
| chr19:45730869-45731067 | Common:1; Rare:43 |