Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:241519667-241520030 | Common:2; Rare:111; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
chr1:241639955-241640054 | Common:1; Rare:35 | ||||
chr1:241640195-241640607 | Common:7; Rare:147 | ||||
chr1:241847762-241848024 | Common:1; Rare:73 | ||||
chr1:241848062-241848289 | Common:2; Rare:49 | ||||
chr1:241848543-241848597 | Rare:5 | ||||
chr1:242524389-242524640 | Common:3; Rare:49 | ||||
chr1:242524683-242524944 | Common:1; Rare:80 | ||||
chr1:243254404-243254633 | Common:4; Rare:46 | ||||
chr1:243254642-243254977 | Common:2; Rare:100 | ||||
chr1:243255009-243255243 | Rare:55 | ||||
chr1:243255310-243255554 | Rare:49 | ||||
chr1:243255776-243256122 | Rare:99; Clinvar:4 | ||||
chr1:243850278-243850464 | Common:2; Rare:56 | ||||
chr1:243850724-243850851 | Rare:47 |