| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34172344-34172570 | Rare:98 | ||||
| chr19:34254484-34254601 | Rare:36 | ||||
| chr19:34365086-34365256 | Common:1; Rare:74 | ||||
| chr19:34428319-34428441 | Rare:52 | ||||
| chr19:34677570-34677758 | Common:4; Rare:55 | ||||
| chr19:34734137-34734273 | Common:1; Rare:40 | ||||
| chr19:35000166-35000473 | Common:4; Rare:75 | ||||
| chr19:35155155-35155230 | Rare:15 | ||||
| chr19:35266946-35267289 | Common:1; Rare:124 | ||||
| chr19:35545454-35545716 | Common:4; Rare:87 | ||||
| chr19:35612696-35612803 | Common:1; Rare:40 | ||||
| chr19:35628816-35629113 | Common:4; Rare:91 | ||||
| chr19:35648110-35648401 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35740485-35740808 | Common:5; Rare:120 | ||||
| chr19:35745397-35745700 | Rare:89 |