Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882012-179882889 | Common:4; Rare:309; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179882902-179883035 | Common:4; Rare:60; Clinvar:2; Clinvar (benign):3 | ||||
chr1:179954447-179954656 | Common:2; Rare:50 | ||||
chr1:179954658-179954899 | Common:1; Rare:53 | ||||
chr1:179955070-179955145 | Rare:16 | ||||
chr1:179955158-179955235 | Rare:21 | ||||
chr1:180154424-180154937 | Common:5; Rare:172 | ||||
chr1:180502272-180503066 | Common:2; Rare:278 | ||||
chr1:180503158-180503479 | Common:3; Rare:71 | ||||
chr1:180631823-180632251 | Common:6; Rare:151 | ||||
chr1:180632316-180632398 | Rare:21 | ||||
chr1:181022685-181022796 | Rare:49 | ||||
chr1:181022800-181023289 | Common:26; Rare:215 | ||||
chr1:181033828-181034019 | Rare:47 | ||||
chr1:181088472-181088827 | Common:1; Rare:130 |