Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:45419362-45419586 | Common:2; Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr20:45898195-45898458 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
chr20:45902265-45902422 | Rare:59 | ||||
chr20:47317343-47317549 | Common:1; Rare:47 | ||||
chr20:47352449-47352650 | Rare:33 | ||||
chr20:47357792-47357898 | Rare:17 | ||||
chr20:47379845-47380034 | Common:1; Rare:25 | ||||
chr20:48760371-48760621 | Rare:51 | ||||
chr20:49114824-49115106 | Common:4; Rare:60 | ||||
chr20:49221159-49221487 | Common:3; Rare:79 | ||||
chr20:49483359-49483560 | Common:3; Rare:50 | ||||
chr20:49539569-49540017 | Common:6; Rare:135 | ||||
chr20:49588414-49588639 | Common:3; Rare:42 | ||||
chr20:49713027-49713356 | Rare:85 | ||||
chr20:49775368-49775602 | Common:2; Rare:40 |