Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:43458264-43458413 | Common:2; Rare:59 | ||||
chr20:43507648-43507720 | Rare:30 | ||||
chr20:43590618-43591010 | Common:1; Rare:91 | ||||
chr20:44210705-44211105 | Common:5; Rare:144 | ||||
chr20:44475772-44475947 | Rare:76 | ||||
chr20:44521998-44522213 | Common:2; Rare:70 | ||||
chr20:44651665-44651854 | Common:1; Rare:49; Clinvar (benign):1 | ||||
chr20:44885566-44885880 | Common:5; Rare:99 | ||||
chr20:44960334-44960566 | Common:1; Rare:91 | ||||
chr20:44966364-44966560 | Common:1; Rare:79 | ||||
chr20:45362956-45363251 | Rare:93 | ||||
chr20:45363353-45363534 | Common:1; Rare:46 | ||||
chr20:45406541-45406732 | Rare:49 | ||||
chr20:45416044-45416154 | Rare:27 | ||||
chr20:45469458-45469770 | Common:1; Rare:80 |