Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21345471-21345674 | Common:2; Rare:75 | ||||
chr1:23019338-23019569 | Rare:85 | ||||
chr1:23692204-23692302 | Rare:34 | ||||
chr1:23778279-23778446 | Common:6; Rare:85 | ||||
chr1:24642951-24643351 | Common:2; Rare:126 | ||||
chr1:25232455-25232642 | Rare:76 | ||||
chr1:25338300-25338403 | Common:1; Rare:39 | ||||
chr1:25819887-25820013 | Common:2; Rare:38 | ||||
chr1:26432112-26432418 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26695619-26695776 | Rare:56 | ||||
chr1:26695937-26696031 | Rare:34 | ||||
chr1:27392378-27392693 | Common:2; Rare:99 | ||||
chr1:28235964-28236179 | Common:3; Rare:68 | ||||
chr1:28505840-28506085 | Common:2; Rare:112 | ||||
chr1:28643018-28643181 | Rare:65 |