Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26695743-26696026 | Common:1; Rare:91 | ||||
chr1:26787865-26788214 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890229-26890336 | Common:1; Rare:44 | ||||
chr1:26899997-26900217 | Rare:88 | ||||
chr1:26900435-26900481 | Rare:17 | ||||
chr1:26960366-26960527 | Common:1; Rare:33 | ||||
chr1:27347956-27347980 | Rare:4 | ||||
chr1:28236067-28236269 | Common:1; Rare:73 | ||||
chr1:28505815-28506047 | Common:2; Rare:88 | ||||
chr1:28552882-28553125 | Common:2; Rare:94 | ||||
chr1:28643002-28643188 | Rare:70 | ||||
chr1:28668679-28668830 | Common:1; Rare:52 | ||||
chr1:28736721-28737065 | Common:3; Rare:112 | ||||
chr1:31296698-31297139 | Common:6; Rare:145 | ||||
chr1:31577893-31578115 | Rare:40 |