Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161505282-161505544 | Common:1; Rare:56 | ||||
chr1:161505761-161506002 | Common:1; Rare:48 | ||||
chr1:161513590-161513834 | Common:1; Rare:38 | ||||
chr1:161549659-161549924 | Common:1; Rare:98 | ||||
chr1:161550089-161550205 | Rare:26 | ||||
chr1:161550961-161550997 | Rare:8 | ||||
chr1:161631098-161631355 | Common:8; Rare:97 | ||||
chr1:161706960-161707262 | Common:3; Rare:63 | ||||
chr1:161749749-161749835 | Rare:36 | ||||
chr1:161766147-161766393 | Common:3; Rare:80 | ||||
chr1:161766430-161766535 | Common:1; Rare:25; Clinvar (pathogenic):1 | ||||
chr1:162023350-162023434 | Common:1; Rare:30; Clinvar (pathogenic):1 | ||||
chr1:162023632-162023966 | Common:1; Rare:96 | ||||
chr1:162497735-162497874 | Common:2; Rare:45 | ||||
chr1:162498036-162498265 | Rare:82 |