| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45091498-45091788 | Common:2; Rare:80 | ||||
| chr19:45178554-45178830 | Common:5; Rare:64; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:45406340-45406649 | Common:1; Rare:67 | ||||
| chr19:45416853-45417051 | Common:1; Rare:35 | ||||
| chr19:45423456-45423951 | Common:5; Rare:110; Clinvar (benign):1 | ||||
| chr19:45450732-45451002 | Common:4; Rare:52 | ||||
| chr19:45468579-45468605 | Rare:5 | ||||
| chr19:45478681-45478815 | Common:2; Rare:78 | ||||
| chr19:45496949-45497271 | Common:2; Rare:97 | ||||
| chr19:45506605-45506635 | Rare:12 | ||||
| chr19:45506818-45506969 | Common:1; Rare:46 | ||||
| chr19:45507228-45507836 | Common:1; Rare:167 | ||||
| chr19:45619241-45619436 | Rare:26 | ||||
| chr19:45667886-45668241 | Common:3; Rare:61 | ||||
| chr19:45691886-45692128 | Rare:84 |