| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:33521753-33521964 | Common:1; Rare:68; Clinvar:5 | ||||
| chr19:34172363-34172612 | Rare:103 | ||||
| chr19:34254513-34254601 | Rare:24 | ||||
| chr19:34365142-34365333 | Common:1; Rare:91; Clinvar (pathogenic):1 | ||||
| chr19:34396298-34396655 | Common:1; Rare:96; Clinvar (pathogenic):1 | ||||
| chr19:34428319-34428517 | Rare:76 | ||||
| chr19:34677233-34677323 | Common:1; Rare:20 | ||||
| chr19:34677572-34677758 | Common:4; Rare:55 | ||||
| chr19:34734222-34734335 | Common:2; Rare:32 | ||||
| chr19:34926807-34927109 | Common:1; Rare:90 | ||||
| chr19:35000195-35000484 | Common:4; Rare:70 | ||||
| chr19:35041550-35041871 | Rare:75 | ||||
| chr19:35138544-35138869 | Rare:74 | ||||
| chr19:35139052-35139776 | Common:7; Rare:157 | ||||
| chr19:35248880-35249091 | Common:1; Rare:101 |