Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38012446-38012766 | Common:1; Rare:83 | ||||
chr1:40257909-40258264 | Common:4; Rare:95; Clinvar:7 | ||||
chr1:42766983-42767297 | Common:4; Rare:102; Clinvar (benign):1 | ||||
chr1:42816972-42817139 | Common:1; Rare:47 | ||||
chr1:42846420-42846638 | Common:1; Rare:57 | ||||
chr1:42958785-42959038 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):3 | ||||
chr1:43172228-43172340 | Common:1; Rare:60 | ||||
chr1:43358840-43359132 | Rare:71 | ||||
chr1:43367990-43368124 | Rare:34 | ||||
chr1:43389754-43389937 | Common:3; Rare:80 | ||||
chr1:43946649-43946969 | Rare:87 | ||||
chr1:43974778-43975041 | Common:3; Rare:71 | ||||
chr1:43978985-43979241 | Common:2; Rare:74 | ||||
chr1:43979836-43980020 | Common:2; Rare:44 | ||||
chr1:44674479-44674712 | Common:2; Rare:56 |