Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236395314-236395436 | Rare:31 | ||||
chr1:236523711-236524769 | Common:13; Rare:436 | ||||
chr1:236604476-236604696 | Common:5; Rare:65 | ||||
chr1:236686291-236686501 | Rare:87 | ||||
chr1:236794985-236795360 | Common:5; Rare:133; Clinvar:2 | ||||
chr1:240091741-240091944 | Common:3; Rare:86 | ||||
chr1:240611680-240612240 | Common:3; Rare:132 | ||||
chr1:241519678-241520036 | Common:2; Rare:105; Clinvar:10; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr1:241640321-241640575 | Common:7; Rare:87 | ||||
chr1:241848068-241848219 | Common:1; Rare:39 | ||||
chr1:241998512-241999102 | Common:1; Rare:215 | ||||
chr1:242524439-242524599 | Common:2; Rare:26 | ||||
chr1:242524890-242525218 | Common:2; Rare:124 | ||||
chr1:243253379-243253844 | Common:4; Rare:108 | ||||
chr1:243254427-243254693 | Common:4; Rare:61 |