Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:63888730-63888920 | Rare:46 | ||||
chr11:64226098-64226334 | Common:3; Rare:67 | ||||
chr11:64240890-64241180 | Rare:79 | ||||
chr11:64284526-64284823 | Rare:114 | ||||
chr11:64317447-64317623 | Common:3; Rare:67 | ||||
chr11:64318044-64318386 | Common:1; Rare:155 | ||||
chr11:64359031-64359194 | Rare:37 | ||||
chr11:64996968-64997109 | Common:1; Rare:16 | ||||
chr11:65014063-65014252 | Rare:41 | ||||
chr11:65084028-65084272 | Common:1; Rare:72 | ||||
chr11:65130467-65130728 | Rare:64; Clinvar (benign):1 | ||||
chr11:65134476-65134570 | Common:1; Rare:25 | ||||
chr11:65181009-65181216 | Common:1; Rare:41 | ||||
chr11:65181221-65181389 | Common:1; Rare:45 | ||||
chr11:65181437-65181772 | Common:2; Rare:108 |