| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50377598-50377868 | Common:1; Rare:101 | ||||
| chr19:50384028-50384389 | Common:2; Rare:151; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50476200-50476583 | Common:1; Rare:179 | ||||
| chr19:50508059-50508262 | Common:1; Rare:45 | ||||
| chr19:50511099-50511385 | Common:2; Rare:101 | ||||
| chr19:50804575-50804913 | Common:7; Rare:105 | ||||
| chr19:51026209-51026336 | Common:2; Rare:32 | ||||
| chr19:51026556-51026683 | Common:1; Rare:37 | ||||
| chr19:51027493-51027656 | Rare:34 | ||||
| chr19:51027660-51027709 | Rare:6 | ||||
| chr19:51108374-51108606 | Common:1; Rare:50 | ||||
| chr19:51366271-51366551 | Common:5; Rare:85; Clinvar (benign):2 | ||||
| chr19:51751846-51751987 | Common:2; Rare:31 | ||||
| chr19:51887866-51888052 | Rare:65 | ||||
| chr19:51927324-51927487 | Common:1; Rare:49 |