Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:176207477-176207670 | Common:1; Rare:75 | ||||
chr1:178725142-178725359 | Common:10; Rare:80 | ||||
chr1:178869246-178869415 | Common:1; Rare:20 | ||||
chr1:179882002-179882325 | Common:4; Rare:76 | ||||
chr1:179882481-179882912 | Rare:213; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179883016-179883132 | Common:3; Rare:47 | ||||
chr1:179954722-179954810 | Rare:21 | ||||
chr1:179955074-179955137 | Rare:13 | ||||
chr1:181088494-181088704 | Rare:67 | ||||
chr1:182789598-182789789 | Common:2; Rare:62 | ||||
chr1:183186127-183186281 | Common:2; Rare:24; Clinvar (benign):2 | ||||
chr1:183472263-183472576 | Common:2; Rare:104 | ||||
chr1:183635635-183636109 | Common:5; Rare:133 | ||||
chr1:183636365-183636474 | Rare:15 | ||||
chr1:184754589-184754698 | Common:1; Rare:49 |