Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42462996-42463372 | Common:4; Rare:121 | ||||
chr1:42682132-42682442 | Common:2; Rare:81 | ||||
chr1:42766546-42766722 | Rare:45; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:42767010-42767303 | Common:4; Rare:92; Clinvar (benign):1 | ||||
chr1:42816985-42817134 | Common:1; Rare:39 | ||||
chr1:42817188-42817454 | Rare:93 | ||||
chr1:42846401-42846638 | Common:1; Rare:65 | ||||
chr1:42958830-42959042 | Common:3; Rare:59; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43172228-43172341 | Common:1; Rare:60 | ||||
chr1:43358674-43359006 | Common:7; Rare:103 | ||||
chr1:43367981-43368208 | Rare:62 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 | ||||
chr1:43649869-43650197 | Rare:78 | ||||
chr1:43946622-43946983 | Rare:98 | ||||
chr1:44674398-44674733 | Common:3; Rare:92 |