Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42682157-42682442 | Common:2; Rare:72 | ||||
chr1:42766978-42767309 | Common:4; Rare:113; Clinvar (benign):1 | ||||
chr1:42817009-42817141 | Common:1; Rare:35 | ||||
chr1:42846391-42846638 | Common:1; Rare:69 | ||||
chr1:42958849-42959051 | Common:1; Rare:51; Clinvar:4; Clinvar (benign):2 | ||||
chr1:43172135-43172353 | Common:3; Rare:91 | ||||
chr1:43358674-43359096 | Common:7; Rare:129 | ||||
chr1:43367927-43368190 | Rare:65 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 | ||||
chr1:43649963-43650173 | Rare:55 | ||||
chr1:43707332-43707592 | Common:2; Rare:79 | ||||
chr1:44674406-44674716 | Common:3; Rare:86 | ||||
chr1:44739674-44739926 | Common:1; Rare:98 | ||||
chr1:44775462-44775599 | Rare:53 | ||||
chr1:44775847-44776140 | Common:2; Rare:108 |