Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26233854-26234318 | Common:6; Rare:134 | ||||
chr1:26234385-26234569 | Common:2; Rare:60 | ||||
chr1:26279824-26280180 | Rare:193 | ||||
chr1:26306528-26306937 | Common:14; Rare:113 | ||||
chr1:26307146-26307292 | Rare:17 | ||||
chr1:26307342-26307750 | Common:6; Rare:59 | ||||
chr1:26317755-26318064 | Common:3; Rare:58 | ||||
chr1:26318262-26318320 | Rare:9 | ||||
chr1:26318680-26318952 | Rare:37 | ||||
chr1:26432018-26432449 | Common:5; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472192-26472639 | Common:4; Rare:153 | ||||
chr1:26472746-26472905 | Common:1; Rare:52 | ||||
chr1:26472989-26473296 | Common:1; Rare:157 | ||||
chr1:26541871-26542658 | Common:3; Rare:144 | ||||
chr1:26543110-26543397 | Common:1; Rare:66 |