| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:33797898-33798091 | Common:4; Rare:51 | ||||
| chr19:34172363-34172575 | Rare:90 | ||||
| chr19:34254473-34254601 | Rare:42 | ||||
| chr19:34365085-34365259 | Common:1; Rare:76 | ||||
| chr19:34404308-34404431 | Common:2; Rare:46 | ||||
| chr19:34428299-34428453 | Common:1; Rare:62 | ||||
| chr19:34677230-34677347 | Common:1; Rare:27 | ||||
| chr19:34677476-34677811 | Common:7; Rare:95 | ||||
| chr19:34734137-34734280 | Common:1; Rare:44 | ||||
| chr19:34926823-34927109 | Common:1; Rare:85 | ||||
| chr19:35545441-35545712 | Common:4; Rare:87 | ||||
| chr19:35628876-35629147 | Common:4; Rare:80 | ||||
| chr19:35648093-35648393 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35740485-35740861 | Common:6; Rare:137 | ||||
| chr19:35745397-35745710 | Rare:91 |