Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:118607275-118607621 | Common:2; Rare:45 | ||||
chr11:118790894-118791259 | Rare:105 | ||||
chr11:118997956-118998200 | Common:4; Rare:82 | ||||
chr11:119018280-119018452 | Common:6; Rare:71 | ||||
chr11:119018626-119018789 | Common:5; Rare:68 | ||||
chr11:119057127-119057460 | Common:3; Rare:133 | ||||
chr11:119067730-119067826 | Rare:35 | ||||
chr11:119168652-119168774 | Rare:23 | ||||
chr11:119206191-119206318 | Common:4; Rare:55; Clinvar:5; Clinvar (benign):3 | ||||
chr11:119317106-119317275 | Rare:57 | ||||
chr11:120138080-120138367 | Common:2; Rare:64 | ||||
chr11:123062109-123062344 | Rare:91 | ||||
chr11:123062398-123062663 | Common:4; Rare:121 | ||||
chr11:124673682-124673926 | Common:4; Rare:80 | ||||
chr11:124762240-124762441 | Rare:54 |