Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42816986-42817136 | Common:1; Rare:39 | ||||
chr1:42846392-42846634 | Common:1; Rare:66 | ||||
chr1:42958846-42959070 | Common:2; Rare:60; Clinvar:4; Clinvar (benign):3 | ||||
chr1:43358706-43359006 | Common:7; Rare:95 | ||||
chr1:43367989-43368180 | Rare:48 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 | ||||
chr1:43946616-43946970 | Rare:96 | ||||
chr1:43974763-43974972 | Common:3; Rare:60 | ||||
chr1:44674406-44674734 | Common:3; Rare:86 | ||||
chr1:44739667-44739887 | Common:1; Rare:83 | ||||
chr1:44775457-44775610 | Rare:59 | ||||
chr1:44775847-44776140 | Common:2; Rare:108 | ||||
chr1:44776404-44776743 | Rare:104 | ||||
chr1:44986560-44986799 | Common:1; Rare:45 | ||||
chr1:45340109-45340170 | Rare:22 |