| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34254466-34254601 | Rare:47 | ||||
| chr19:34365086-34365246 | Common:1; Rare:70 | ||||
| chr19:34428319-34428435 | Rare:50 | ||||
| chr19:34677554-34677751 | Common:5; Rare:56 | ||||
| chr19:34734141-34734274 | Common:1; Rare:39 | ||||
| chr19:34926844-34926913 | Common:1; Rare:31 | ||||
| chr19:35155155-35155230 | Rare:15 | ||||
| chr19:35545468-35545712 | Common:4; Rare:79 | ||||
| chr19:35628827-35629141 | Common:5; Rare:93 | ||||
| chr19:35648110-35648392 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35740470-35740825 | Common:6; Rare:127 | ||||
| chr19:35745397-35745695 | Rare:88 | ||||
| chr19:35748286-35748629 | Common:3; Rare:99 | ||||
| chr19:35757857-35758204 | Common:2; Rare:103 | ||||
| chr19:35900538-35900661 | Rare:28 |