Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26545658-26545938 | Common:1; Rare:64 | ||||
chr1:26695361-26695660 | Common:1; Rare:83 | ||||
chr1:26695661-26696134 | Common:1; Rare:150 | ||||
chr1:26696700-26696824 | Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
chr1:26786942-26787114 | Rare:38 | ||||
chr1:26787326-26787736 | Common:1; Rare:108 | ||||
chr1:26787809-26788345 | Common:3; Rare:152; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26788530-26788646 | Rare:23 | ||||
chr1:26789202-26789262 | Rare:14 | ||||
chr1:26826415-26826830 | Rare:111 | ||||
chr1:26826946-26827093 | Rare:31 | ||||
chr1:26827117-26827137 | Rare:3 | ||||
chr1:26890151-26890454 | Common:2; Rare:114 | ||||
chr1:26900039-26900224 | Rare:70 | ||||
chr1:26900386-26900586 | Rare:79 |