Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21887215-21887675 | Common:3; Rare:176; Clinvar:13; Clinvar (benign):3 | ||||
chr1:22025181-22025532 | Common:7; Rare:90 | ||||
chr1:23369954-23369993 | Rare:4 | ||||
chr1:25875481-25875676 | Rare:59 | ||||
chr1:26160738-26160983 | Rare:44 | ||||
chr1:26942657-26942895 | Rare:87 | ||||
chr1:27428760-27429117 | Common:2; Rare:80 | ||||
chr1:28581840-28582027 | Common:1; Rare:62 | ||||
chr1:28648333-28648629 | Common:5; Rare:110 | ||||
chr1:31580516-31580834 | Rare:77 | ||||
chr1:32036680-32036964 | Common:4; Rare:52 | ||||
chr1:32240310-32240541 | Common:2; Rare:46 | ||||
chr1:33346961-33347253 | Common:1; Rare:51 | ||||
chr1:36386535-36386702 | Rare:23 | ||||
chr1:39410992-39411100 | Rare:23 |