Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:119018280-119018819 | Common:13; Rare:208 | ||||
chr11:119057110-119057446 | Common:3; Rare:132 | ||||
chr11:119067632-119067821 | Common:3; Rare:64 | ||||
chr11:119121274-119121647 | Common:1; Rare:90 | ||||
chr11:119206175-119206391 | Common:5; Rare:98; Clinvar:8; Clinvar (benign):4 | ||||
chr11:119317106-119317248 | Rare:51 | ||||
chr11:121292586-121292786 | Rare:65; Clinvar:3 | ||||
chr11:122882692-122882939 | Common:1; Rare:67 | ||||
chr11:123062076-123062339 | Common:3; Rare:109 | ||||
chr11:123062408-123062679 | Common:4; Rare:123 | ||||
chr11:123741612-123741683 | Common:1; Rare:26 | ||||
chr11:124673712-124673940 | Common:4; Rare:67 | ||||
chr11:124762256-124762441 | Rare:48 | ||||
chr11:124800372-124800481 | Rare:43 | ||||
chr11:124953989-124954202 | Common:4; Rare:59 |