Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113929516-113929650 | Common:1; Rare:33 | ||||
chr1:114716700-114717060 | Common:4; Rare:130; Clinvar:5; Clinvar (benign):1 | ||||
chr1:117367335-117367468 | Common:2; Rare:41 | ||||
chr1:117929612-117929811 | Common:3; Rare:52 | ||||
chr1:119140644-119140768 | Common:1; Rare:37 | ||||
chr1:145823919-145824219 | Rare:104 | ||||
chr1:145859005-145859191 | Rare:52 | ||||
chr1:145918658-145919009 | Common:2; Rare:84; Clinvar:1 | ||||
chr1:145927477-145927612 | Rare:31 | ||||
chr1:145964575-145964737 | Rare:41 | ||||
chr1:145996454-145996740 | Common:1; Rare:109 | ||||
chr1:149886679-149886919 | Rare:64 | ||||
chr1:150067665-150067840 | Rare:49 | ||||
chr1:150629549-150629853 | Common:1; Rare:64 | ||||
chr1:150697119-150697319 | Common:1; Rare:43 |