| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44808090-44808420 | Common:1; Rare:53 | ||||
| chr19:44811920-44812634 | Common:10; Rare:356; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:44844732-44845075 | Common:3; Rare:200 | ||||
| chr19:44847524-44847835 | Common:4; Rare:147 | ||||
| chr19:44847800-44848150 | Common:1; Rare:124 | ||||
| chr19:44865001-44865684 | Common:7; Rare:333 | ||||
| chr19:45075557-45075798 | Common:1; Rare:61 | ||||
| chr19:45098280-45098680 | Common:3; Rare:147 | ||||
| chr19:45112557-45113201 | Common:6; Rare:206 | ||||
| chr19:45113659-45114013 | Common:8; Rare:157 | ||||
| chr19:45117180-45117470 | Common:8; Rare:111 | ||||
| chr19:45117660-45118380 | Common:2; Rare:313 | ||||
| chr19:45119659-45120059 | Common:1; Rare:101 | ||||
| chr19:45122070-45122360 | Common:1; Rare:102 | ||||
| chr19:45123404-45123810 | Common:1; Rare:117 |