Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174159981-174160007 | Common:1; Rare:4 | ||||
chr1:174999344-174999483 | Common:1; Rare:38 | ||||
chr1:174999679-175000156 | Common:3; Rare:155 | ||||
chr1:175023388-175023597 | Common:1; Rare:60 | ||||
chr1:176207463-176207691 | Common:2; Rare:88 | ||||
chr1:178094392-178094624 | Common:1; Rare:90 | ||||
chr1:178341318-178341539 | Common:1; Rare:44 | ||||
chr1:178725114-178725316 | Common:10; Rare:76 | ||||
chr1:178869231-178869369 | Common:1; Rare:19 | ||||
chr1:178871023-178871295 | Rare:51 | ||||
chr1:179229670-179229822 | Common:3; Rare:21 | ||||
chr1:179293664-179293894 | Common:3; Rare:74 | ||||
chr1:179877756-179877934 | Rare:37 | ||||
chr1:179882147-179882324 | Common:1; Rare:34 | ||||
chr1:179882475-179882879 | Rare:194; Clinvar:8; Clinvar (benign):2 |