Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42767023-42767293 | Common:4; Rare:81 | ||||
chr1:42817009-42817136 | Common:1; Rare:32 | ||||
chr1:42817263-42817588 | Rare:102 | ||||
chr1:42846401-42846642 | Common:1; Rare:67 | ||||
chr1:42958792-42959084 | Common:4; Rare:80; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172233-43172344 | Common:1; Rare:60 | ||||
chr1:43358674-43359011 | Common:7; Rare:104 | ||||
chr1:43367993-43368219 | Rare:59 | ||||
chr1:43389768-43389950 | Common:3; Rare:77 | ||||
chr1:43649859-43650177 | Rare:78 | ||||
chr1:43946548-43946983 | Rare:116 | ||||
chr1:44031433-44031676 | Common:2; Rare:49 | ||||
chr1:44674451-44674716 | Common:2; Rare:62 | ||||
chr1:44739648-44739873 | Common:2; Rare:83 | ||||
chr1:44775453-44775607 | Rare:58 |