Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:52706353-52706689 | Common:1; Rare:89 | ||||
chr3:52834793-52835126 | Common:1; Rare:87 | ||||
chr3:52843159-52843451 | Common:3; Rare:66 | ||||
chr3:53347518-53347734 | Common:1; Rare:68 | ||||
chr3:53891787-53892035 | Common:2; Rare:74 | ||||
chr3:56557084-56557238 | Common:2; Rare:60 | ||||
chr3:57227604-57227899 | Common:3; Rare:101 | ||||
chr3:57292649-57292917 | Common:2; Rare:37 | ||||
chr3:57556012-57556331 | Rare:77 | ||||
chr3:57597330-57597667 | Common:4; Rare:105 | ||||
chr3:58433799-58433945 | Rare:57; Clinvar (benign):3 | ||||
chr3:61251383-61251597 | Common:4; Rare:53 | ||||
chr3:61561412-61561656 | Common:2; Rare:86 | ||||
chr3:63863734-63864126 | Common:7; Rare:131 | ||||
chr3:64687583-64687719 | Rare:37 |