Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26472894-26473251 | Common:1; Rare:156 | ||||
chr1:26543046-26543207 | Common:1; Rare:39 | ||||
chr1:26545696-26545926 | Common:1; Rare:50 | ||||
chr1:26695613-26695721 | Rare:36 | ||||
chr1:26787868-26788214 | Common:3; Rare:98; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26831872-26832083 | Rare:35 | ||||
chr1:26890193-26890377 | Common:1; Rare:71 | ||||
chr1:26900060-26900217 | Rare:62 | ||||
chr1:26900417-26900553 | Rare:49 | ||||
chr1:26921549-26921904 | Common:3; Rare:112 | ||||
chr1:26945458-26945612 | Rare:49 | ||||
chr1:27366912-27367248 | Common:1; Rare:67 | ||||
chr1:27490025-27490324 | Rare:102 | ||||
chr1:27626047-27626342 | Common:2; Rare:45 | ||||
chr1:27626492-27626772 | Common:1; Rare:50 |