Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:118607361-118607652 | Common:1; Rare:48 | ||||
chr11:118621165-118621516 | Rare:72 | ||||
chr11:118790894-118791259 | Rare:105 | ||||
chr11:118910391-118910712 | Common:3; Rare:101 | ||||
chr11:118997980-118998185 | Common:4; Rare:60 | ||||
chr11:119018280-119018452 | Common:6; Rare:71 | ||||
chr11:119018640-119018795 | Common:5; Rare:68 | ||||
chr11:119057074-119057448 | Common:3; Rare:148 | ||||
chr11:119067624-119067821 | Common:3; Rare:65 | ||||
chr11:119084792-119084939 | Common:1; Rare:43; Clinvar (benign):1 | ||||
chr11:119206186-119206373 | Common:5; Rare:82; Clinvar:7; Clinvar (benign):4 | ||||
chr11:119317110-119317275 | Rare:57 | ||||
chr11:120325229-120325344 | Common:1; Rare:29 | ||||
chr11:120336314-120336578 | Rare:102 | ||||
chr11:121292569-121292793 | Rare:76; Clinvar:3 |