Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174999795-175000158 | Common:3; Rare:127 | ||||
chr1:175023409-175023641 | Common:1; Rare:60 | ||||
chr1:178725143-178725397 | Common:10; Rare:87 | ||||
chr1:179025722-179026022 | Common:4; Rare:78 | ||||
chr1:179081887-179082114 | Common:1; Rare:70 | ||||
chr1:179229626-179229846 | Common:7; Rare:56 | ||||
chr1:179293701-179293934 | Common:3; Rare:65 | ||||
chr1:179877739-179877930 | Rare:38 | ||||
chr1:179882129-179882311 | Common:1; Rare:33 | ||||
chr1:179882482-179882958 | Common:1; Rare:237; Clinvar:10; Clinvar (benign):4 | ||||
chr1:179883005-179883159 | Common:3; Rare:60 | ||||
chr1:179954703-179954814 | Rare:25 | ||||
chr1:180502032-180502657 | Common:1; Rare:228 | ||||
chr1:180631987-180632228 | Common:2; Rare:98 | ||||
chr1:181022801-181022972 | Common:1; Rare:79 |