| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19320480-19320870 | Common:4; Rare:142 | ||||
| chr19:19516147-19516307 | Rare:103; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19668669-19668849 | Common:1; Rare:52 | ||||
| chr19:21082065-21082288 | Rare:51 | ||||
| chr19:21141900-21142085 | Rare:50 | ||||
| chr19:24033302-24033558 | Common:7; Rare:56 | ||||
| chr19:29213087-29213239 | Common:3; Rare:52 | ||||
| chr19:29606163-29606324 | Rare:53 | ||||
| chr19:29665251-29665466 | Common:4; Rare:78 | ||||
| chr19:29715202-29715332 | Common:1; Rare:55 | ||||
| chr19:29942130-29942241 | Rare:45 | ||||
| chr19:32345528-32345689 | Common:1; Rare:54 | ||||
| chr19:32405541-32405835 | Common:1; Rare:125 | ||||
| chr19:32405865-32406156 | Common:2; Rare:90 | ||||
| chr19:32580984-32581326 | Common:5; Rare:127 |