Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:133309148-133309386 | Common:2; Rare:82 | ||||
chr10:133565533-133565875 | Common:5; Rare:122 | ||||
chr11:207320-207719 | Common:8; Rare:134 | ||||
chr11:208508-208865 | Common:1; Rare:111 | ||||
chr11:236333-236535 | Common:7; Rare:63 | ||||
chr11:236876-237052 | Common:1; Rare:65 | ||||
chr11:407110-407395 | Common:7; Rare:86 | ||||
chr11:417344-417487 | Rare:35 | ||||
chr11:506732-506981 | Common:3; Rare:86 | ||||
chr11:507122-507373 | Common:1; Rare:77 | ||||
chr11:560710-561016 | Common:5; Rare:142 | ||||
chr11:576422-576531 | Rare:44 | ||||
chr11:615946-616108 | Common:1; Rare:50 | ||||
chr11:695639-695830 | Rare:49 | ||||
chr11:764014-764430 | Common:2; Rare:112; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |