Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:133149116-133149304 | Common:2; Rare:56 | ||||
chr4:139556180-139556302 | Rare:28 | ||||
chr4:140373371-140373713 | Common:3; Rare:136 | ||||
chr4:140756350-140756433 | Rare:21 | ||||
chr4:143184669-143184985 | Common:8; Rare:124 | ||||
chr4:145098165-145098348 | Rare:63 | ||||
chr4:145619328-145619404 | Rare:28; Clinvar (benign):1 | ||||
chr4:150581765-150581941 | Rare:34 | ||||
chr4:151015708-151015788 | Rare:32 | ||||
chr4:152779758-152780169 | Common:2; Rare:102 | ||||
chr4:158172647-158172824 | Common:1; Rare:31 | ||||
chr4:158671849-158672329 | Common:5; Rare:116; Clinvar:2; Clinvar (benign):1 | ||||
chr4:168480485-168480567 | Rare:11 | ||||
chr4:169620411-169620593 | Common:2; Rare:69 | ||||
chr4:173370690-173370994 | Common:2; Rare:78 |