Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:206612440-206612643 | Common:3; Rare:55 | ||||
chr1:207052986-207053295 | Common:1; Rare:78 | ||||
chr1:207751923-207752179 | Common:1; Rare:80 | ||||
chr1:208244225-208244540 | Common:1; Rare:89 | ||||
chr1:209784531-209784721 | Common:1; Rare:62 | ||||
chr1:209937962-209938274 | Common:3; Rare:106; Clinvar (pathogenic):1 | ||||
chr1:211259057-211259563 | Common:2; Rare:177 | ||||
chr1:211259733-211259970 | Rare:67 | ||||
chr1:211675579-211675737 | Rare:34 | ||||
chr1:212035497-212035801 | Common:2; Rare:84 | ||||
chr1:212414833-212414961 | Common:2; Rare:42 | ||||
chr1:212432769-212433072 | Rare:82 | ||||
chr1:212791741-212791930 | Common:4; Rare:81 | ||||
chr1:212792463-212792528 | Common:2; Rare:21 | ||||
chr1:212858089-212858295 | Common:3; Rare:52; Clinvar:1 |