Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:3795705-3795789 | Common:2; Rare:25 | ||||
chr20:4148562-4148861 | Rare:83 | ||||
chr20:5112854-5113212 | Common:1; Rare:131 | ||||
chr20:5119891-5120174 | Common:1; Rare:95 | ||||
chr20:5126699-5127083 | Common:3; Rare:132 | ||||
chr20:5610902-5611144 | Common:2; Rare:83 | ||||
chr20:5950410-5950689 | Common:8; Rare:86 | ||||
chr20:11890775-11890892 | Common:1; Rare:51 | ||||
chr20:13784884-13785061 | Common:2; Rare:73; Clinvar (benign):2 | ||||
chr20:16573315-16573527 | Common:1; Rare:54 | ||||
chr20:17968406-17968599 | Common:4; Rare:77 | ||||
chr20:17968795-17969090 | Common:2; Rare:111 | ||||
chr20:20017193-20017403 | Rare:71 | ||||
chr20:21303235-21303456 | Rare:74 | ||||
chr20:24992702-24992835 | Common:4; Rare:59 |