Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:118401320-118401717 | Rare:133 | ||||
chr11:118531145-118531237 | Rare:36 | ||||
chr11:118565851-118566152 | Common:1; Rare:62 | ||||
chr11:118572365-118572528 | Rare:56 | ||||
chr11:118621269-118621524 | Rare:55 | ||||
chr11:118790888-118791249 | Rare:105 | ||||
chr11:118997977-118998185 | Common:4; Rare:62 | ||||
chr11:119018282-119018566 | Common:8; Rare:115 | ||||
chr11:119018589-119018817 | Common:5; Rare:89 | ||||
chr11:119057057-119057481 | Common:3; Rare:162 | ||||
chr11:119067636-119067846 | Common:3; Rare:71 | ||||
chr11:119101797-119102025 | Rare:62; Clinvar:4 | ||||
chr11:119206211-119206369 | Common:4; Rare:69; Clinvar:7; Clinvar (benign):4 | ||||
chr11:119729184-119729351 | Rare:42 | ||||
chr11:123062438-123062632 | Common:2; Rare:82 |