Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:218345228-218345405 | Common:1; Rare:30; Clinvar (benign):1 | ||||
chr1:220253266-220253597 | Common:2; Rare:71 | ||||
chr1:223992547-223992858 | Common:4; Rare:111 | ||||
chr1:229431539-229432191 | Common:6; Rare:173; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):5 | ||||
chr1:229432268-229432677 | Common:4; Rare:98; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):4 | ||||
chr1:229432861-229432995 | Common:4; Rare:49; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:229563730-229563938 | Common:2; Rare:24 | ||||
chr1:246569747-246569868 | Common:1; Rare:22 | ||||
chr10:3783486-3783522 | Rare:6 | ||||
chr10:7541195-7541523 | Common:6; Rare:64 | ||||
chr10:8052807-8053009 | Common:3; Rare:45 | ||||
chr10:19728514-19728550 | Rare:9 | ||||
chr10:21292998-21293072 | Rare:13 | ||||
chr10:22251815-22252099 | Rare:62 | ||||
chr10:24118390-24118537 | Rare:36 |