Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32464753-32465102 | Rare:83 | ||||
chr1:32539220-32539500 | Rare:54 | ||||
chr1:32650446-32650669 | Common:1; Rare:93 | ||||
chr1:32650984-32651316 | Common:1; Rare:129 | ||||
chr1:32741281-32742050 | Common:4; Rare:246 | ||||
chr1:32753760-32754180 | Common:4; Rare:148 | ||||
chr1:32816823-32816963 | Rare:24 | ||||
chr1:32817291-32817692 | Common:1; Rare:101; Clinvar:5; Clinvar (benign):2 | ||||
chr1:32818119-32818311 | Common:1; Rare:58 | ||||
chr1:32893251-32893906 | Common:3; Rare:366; Clinvar (pathogenic):1 | ||||
chr1:32964805-32965025 | Common:2; Rare:83 | ||||
chr1:33036842-33037123 | Rare:96 | ||||
chr1:33080916-33081189 | Common:2; Rare:72 | ||||
chr1:33182023-33182231 | Rare:46 | ||||
chr1:33255599-33257102 | Common:14; Rare:575 |