| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44356672-44356820 | Common:1; Rare:25 | ||||
| chr19:44643793-44643959 | Rare:47 | ||||
| chr19:44808950-44809125 | Rare:61 | ||||
| chr19:45038951-45039087 | Rare:44 | ||||
| chr19:45322796-45323029 | Common:2; Rare:40 | ||||
| chr19:45323092-45323158 | Common:1; Rare:13 | ||||
| chr19:45385560-45385946 | Rare:132 | ||||
| chr19:45406290-45406680 | Common:2; Rare:93 | ||||
| chr19:45507386-45507516 | Rare:39 | ||||
| chr19:45639362-45639712 | Common:3; Rare:82 | ||||
| chr19:45692383-45692690 | Common:1; Rare:68 | ||||
| chr19:46298120-46298473 | Common:5; Rare:85 | ||||
| chr19:46346941-46347217 | Common:3; Rare:94 | ||||
| chr19:46600984-46601436 | Common:5; Rare:155; Clinvar (benign):3 | ||||
| chr19:46608292-46608531 | Common:1; Rare:58; Clinvar (benign):5 |