Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:117986305-117986447 | Common:2; Rare:54; Clinvar:2 | ||||
chr11:118401058-118401710 | Common:1; Rare:204 | ||||
chr11:118790877-118791291 | Rare:133 | ||||
chr11:118925415-118925422 | |||||
chr11:118997977-118998264 | Common:4; Rare:96 | ||||
chr11:119018268-119018452 | Common:6; Rare:73 | ||||
chr11:119018626-119018795 | Common:5; Rare:71 | ||||
chr11:119057110-119057481 | Common:3; Rare:145 | ||||
chr11:119067630-119067874 | Common:3; Rare:83 | ||||
chr11:119206180-119206391 | Common:5; Rare:95; Clinvar:8; Clinvar (benign):4 | ||||
chr11:119311363-119311638 | Rare:98 | ||||
chr11:119317087-119317275 | Rare:62 | ||||
chr11:119381607-119381824 | Common:1; Rare:44 | ||||
chr11:120336119-120336484 | Rare:148 | ||||
chr11:123062062-123062339 | Common:5; Rare:120 |