Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49119071-49119177 | Rare:35 | ||||
chr19:49155353-49155551 | Rare:36 | ||||
chr19:49157634-49157859 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
chr19:49335139-49335545 | Common:1; Rare:85 | ||||
chr19:49362347-49362474 | Rare:34 | ||||
chr19:49453094-49453322 | Common:1; Rare:70 | ||||
chr19:49453480-49453599 | Rare:35 | ||||
chr19:49474161-49474271 | Common:1; Rare:23 | ||||
chr19:49487272-49487644 | Common:5; Rare:131 | ||||
chr19:49495981-49496537 | Common:3; Rare:198 | ||||
chr19:49513124-49513467 | Common:1; Rare:76 | ||||
chr19:49527864-49528034 | Common:3; Rare:52 | ||||
chr19:49560720-49560814 | Rare:23 | ||||
chr19:49580527-49580656 | Rare:44 | ||||
chr19:49581287-49581424 | Common:1; Rare:27 |