Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48807246-48807369 | Common:1; Rare:27 | ||||
chr19:48810836-48811119 | Rare:87 | ||||
chr19:48859367-48859454 | Rare:20 | ||||
chr19:48860104-48860323 | Common:1; Rare:54 | ||||
chr19:48868223-48868697 | Common:1; Rare:89 | ||||
chr19:48872090-48872427 | Common:3; Rare:88 | ||||
chr19:48896141-48896466 | Common:3; Rare:84 | ||||
chr19:48900151-48900400 | Common:1; Rare:79 | ||||
chr19:48933508-48933722 | Common:3; Rare:67 | ||||
chr19:48954643-48954931 | Common:1; Rare:103 | ||||
chr19:48965001-48965408 | Common:1; Rare:103; Clinvar (pathogenic):5 | ||||
chr19:48993167-48993596 | Common:4; Rare:182; Clinvar:3; Clinvar (benign):3 | ||||
chr19:48993762-48993942 | Common:4; Rare:61 | ||||
chr19:49085091-49085634 | Common:3; Rare:208 | ||||
chr19:49119128-49119386 | Rare:82 |