Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53946253-53946497 | Common:1; Rare:87 | ||||
chr1:54053189-54053654 | Common:6; Rare:155 | ||||
chr1:54199993-54200229 | Rare:60 | ||||
chr1:54887120-54887350 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):1 | ||||
chr1:58700053-58700170 | Common:4; Rare:50 | ||||
chr1:58784020-58784176 | Rare:32 | ||||
chr1:59296520-59296849 | Common:12; Rare:88 | ||||
chr1:61725083-61725177 | Rare:60 | ||||
chr1:62688277-62688500 | Common:1; Rare:93 | ||||
chr1:62784070-62784180 | Rare:44 | ||||
chr1:63367479-63367679 | Rare:61; Clinvar (benign):1 | ||||
chr1:63523161-63523602 | Common:3; Rare:119 | ||||
chr1:63593624-63593675 | Rare:27; Clinvar (pathogenic):1 | ||||
chr1:66533553-66533615 | Rare:5 | ||||
chr1:66752329-66752494 | Rare:35 |