Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:38012524-38012799 | Rare:83 | ||||
chr1:38873297-38873563 | Common:3; Rare:93 | ||||
chr1:39026291-39026418 | Common:1; Rare:35 | ||||
chr1:40161254-40161395 | Rare:36 | ||||
chr1:40257915-40258338 | Common:4; Rare:124; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40508694-40508794 | Common:3; Rare:27 | ||||
chr1:40691508-40691639 | Common:1; Rare:66 | ||||
chr1:40692036-40692318 | Common:1; Rare:85 | ||||
chr1:42456214-42456575 | Common:1; Rare:105 | ||||
chr1:42766993-42767301 | Common:4; Rare:102; Clinvar (benign):1 | ||||
chr1:42816976-42817134 | Common:1; Rare:43 | ||||
chr1:42846392-42846640 | Common:1; Rare:68 | ||||
chr1:42958660-42959046 | Common:3; Rare:98; Clinvar:5; Clinvar (benign):7 | ||||
chr1:43172214-43172335 | Common:1; Rare:59 | ||||
chr1:43358690-43359019 | Common:7; Rare:104 |