| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49676292-49676571 | Common:2; Rare:60 | ||||
| chr19:49677047-49677365 | Common:3; Rare:98 | ||||
| chr19:49678285-49678590 | Common:1; Rare:44 | ||||
| chr19:49766184-49766528 | Rare:101 | ||||
| chr19:49809275-49809376 | Rare:25 | ||||
| chr19:49813258-49813394 | Common:1; Rare:48 | ||||
| chr19:49813674-49813731 | Rare:17 | ||||
| chr19:49817467-49817638 | Common:2; Rare:45 | ||||
| chr19:49818188-49818391 | Common:4; Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:49818421-49818609 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:49850590-49850767 | Rare:47 | ||||
| chr19:49851016-49851261 | Common:1; Rare:103 | ||||
| chr19:49867175-49867412 | Common:2; Rare:84; Clinvar:2; Clinvar (benign):6 | ||||
| chr19:49867486-49867736 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:49876162-49876361 | Rare:62 |