Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:2115325-2115598 | Common:4; Rare:87 | ||||
chr19:3552922-3553077 | Rare:23 | ||||
chr19:3554535-3554868 | Common:3; Rare:53 | ||||
chr19:3558189-3558336 | Rare:30 | ||||
chr19:3963670-3963916 | Common:5; Rare:76 | ||||
chr19:3977271-3977461 | Common:2; Rare:68; Clinvar (benign):1 | ||||
chr19:4363844-4364127 | Common:2; Rare:93 | ||||
chr19:13167585-13167697 | Rare:33 | ||||
chr19:14140100-14140330 | Common:1; Rare:31 | ||||
chr19:14496676-14496839 | Rare:26 | ||||
chr19:14565950-14566083 | Common:1; Rare:54 | ||||
chr19:14809288-14809427 | Common:1; Rare:26 | ||||
chr19:14830830-14831014 | Rare:40 | ||||
chr19:17125258-17125553 | Common:5; Rare:65 | ||||
chr19:17151438-17151701 | Common:2; Rare:40 |