Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155008490-155008986 | Rare:101 | ||||
chr1:155227529-155227735 | Common:1; Rare:57 | ||||
chr1:156130320-156130764 | Common:3; Rare:111; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:156700872-156701249 | Common:3; Rare:93 | ||||
chr1:156748331-156748487 | Common:2; Rare:26 | ||||
chr1:160408055-160408402 | Common:1; Rare:64 | ||||
chr1:160999881-161000196 | Common:1; Rare:71 | ||||
chr1:161530888-161531107 | Common:5; Rare:82 | ||||
chr1:167454986-167455076 | Rare:19 | ||||
chr1:169111210-169111506 | Rare:79; Clinvar:1 | ||||
chr1:175008401-175008680 | Common:1; Rare:63 | ||||
chr1:178037862-178038021 | Rare:54 | ||||
chr1:181089397-181089747 | Common:4; Rare:136 | ||||
chr1:185316038-185316348 | Common:1; Rare:71 | ||||
chr1:195721619-195721895 | Common:2; Rare:61 |