Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:43770085-43770211 | Common:2; Rare:40 | ||||
chr6:44127365-44127629 | Common:4; Rare:75 | ||||
chr6:44387620-44387729 | Common:2; Rare:33 | ||||
chr6:52995355-52995757 | Common:4; Rare:162 | ||||
chr6:75284734-75285014 | Common:1; Rare:76 | ||||
chr6:79537401-79537623 | Rare:56 | ||||
chr6:83193203-83193389 | Common:3; Rare:62 | ||||
chr6:87155262-87155583 | Rare:84 | ||||
chr6:87589964-87590145 | Common:1; Rare:72; Clinvar (benign):3 | ||||
chr6:89638732-89638851 | Common:3; Rare:37 | ||||
chr6:100881265-100881479 | Common:5; Rare:89 | ||||
chr6:106325676-106325892 | Common:1; Rare:76 | ||||
chr6:109691167-109691296 | Common:1; Rare:29; Clinvar (benign):1 | ||||
chr6:110958686-110958764 | Common:1; Rare:31 | ||||
chr6:112087452-112087684 | Rare:71 |