| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45423467-45423698 | Common:2; Rare:49; Clinvar (benign):1 | ||||
| chr19:45423839-45423952 | Common:2; Rare:31 | ||||
| chr19:45450733-45451031 | Common:4; Rare:56 | ||||
| chr19:45469262-45469472 | Rare:62 | ||||
| chr19:45507228-45507525 | Common:1; Rare:80 | ||||
| chr19:45730847-45731106 | Common:1; Rare:59 | ||||
| chr19:45863090-45863396 | Common:4; Rare:101 | ||||
| chr19:46346939-46347143 | Common:3; Rare:69 | ||||
| chr19:46413419-46413759 | Common:1; Rare:99 | ||||
| chr19:46717080-46717225 | Common:2; Rare:46 | ||||
| chr19:46784774-46785054 | Common:1; Rare:63 | ||||
| chr19:46787262-46787384 | Rare:23 | ||||
| chr19:46850241-46850384 | Rare:20 | ||||
| chr19:47113137-47113430 | Common:1; Rare:78 | ||||
| chr19:47256460-47256585 | Rare:48 |