Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:119094708-119094793 | Common:1; Rare:27 | ||||
chr11:119189188-119189528 | Common:1; Rare:69 | ||||
chr11:119368410-119368563 | Rare:42 | ||||
chr11:123430898-123431134 | Common:1; Rare:85 | ||||
chr11:123488680-123488741 | Common:1; Rare:9 | ||||
chr11:124638675-124638842 | Common:2; Rare:56 | ||||
chr11:129828568-129828603 | Rare:6 | ||||
chr11:129839437-129839633 | Common:1; Rare:36 | ||||
chr11:129854178-129854464 | Rare:39 | ||||
chr11:129857149-129857353 | Common:2; Rare:62 | ||||
chr11:129865047-129865142 | Rare:28 | ||||
chr11:130188442-130188600 | Common:4; Rare:45 | ||||
chr11:130194630-130194826 | Common:3; Rare:66; Clinvar (benign):1 | ||||
chr11:130198348-130198594 | Common:2; Rare:73 | ||||
chr11:130914677-130914848 | Common:7; Rare:61 |