Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:178093972-178094106 | Common:1; Rare:28 | ||||
chr1:178341312-178341520 | Common:1; Rare:39 | ||||
chr1:178725090-178725335 | Common:10; Rare:92 | ||||
chr1:179025677-179025959 | Common:4; Rare:74 | ||||
chr1:179081911-179082134 | Common:1; Rare:69 | ||||
chr1:179229670-179229717 | Rare:5 | ||||
chr1:179293642-179293864 | Common:2; Rare:83 | ||||
chr1:179877743-179877982 | Rare:49 | ||||
chr1:179882129-179882299 | Common:1; Rare:30 | ||||
chr1:179882466-179882878 | Rare:195; Clinvar:8; Clinvar (benign):2 | ||||
chr1:179882995-179883162 | Common:3; Rare:63 | ||||
chr1:179954382-179954601 | Common:2; Rare:56 | ||||
chr1:179954691-179954817 | Rare:29 | ||||
chr1:180154496-180154923 | Common:3; Rare:139 | ||||
chr1:180502454-180502665 | Common:1; Rare:79 |