Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234608624-234608748 | Common:2; Rare:56; Clinvar (benign):1 | ||||
chr1:234610073-234610296 | Common:1; Rare:99 | ||||
chr1:234610380-234610418 | Rare:7 | ||||
chr1:234610854-234611138 | Common:1; Rare:103 | ||||
chr1:234611352-234611725 | Common:2; Rare:94 | ||||
chr1:234612635-234612890 | Common:1; Rare:33 | ||||
chr1:234721959-234722336 | Common:3; Rare:73 | ||||
chr1:234723297-234723469 | Common:1; Rare:36 | ||||
chr1:234723703-234723866 | Common:5; Rare:30 | ||||
chr1:234724716-234724992 | Rare:61 | ||||
chr1:234725449-234725554 | Rare:22 | ||||
chr1:234744002-234744253 | Common:1; Rare:35 | ||||
chr1:234772407-234772588 | Common:1; Rare:37 | ||||
chr1:234918158-234918502 | Common:2; Rare:79 | ||||
chr1:234960790-234960931 | Common:2; Rare:22 |