| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:15107807-15107888 | Rare:11 | ||||
| chr19:15125644-15125750 | Common:1; Rare:22 | ||||
| chr19:16075922-16076136 | Common:6; Rare:75 | ||||
| chr19:16076207-16076697 | Common:2; Rare:132 | ||||
| chr19:16197713-16198002 | Common:3; Rare:95 | ||||
| chr19:16496140-16496424 | Common:2; Rare:76 | ||||
| chr19:16542391-16542574 | Common:2; Rare:49 | ||||
| chr19:16660084-16660380 | Common:3; Rare:113 | ||||
| chr19:17215263-17215408 | Common:2; Rare:54 | ||||
| chr19:17215616-17215797 | Common:3; Rare:51 | ||||
| chr19:17303372-17303463 | Common:1; Rare:24 | ||||
| chr19:17337428-17337585 | Common:1; Rare:30 | ||||
| chr19:17405528-17405847 | Common:6; Rare:60 | ||||
| chr19:17511449-17511625 | Common:3; Rare:72 | ||||
| chr19:17847960-17848141 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 |