Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:107591085-107591330 | Rare:87 | ||||
chr11:108009304-108009349 | Rare:23 | ||||
chr11:108222609-108223128 | Common:1; Rare:161; Clinvar:8; Clinvar (benign):1 | ||||
chr11:111913132-111913266 | Rare:39 | ||||
chr11:112074005-112074343 | Common:1; Rare:70 | ||||
chr11:112086729-112086899 | Rare:68 | ||||
chr11:113314454-113314616 | Rare:58 | ||||
chr11:114400434-114400737 | Common:2; Rare:124 | ||||
chr11:117232555-117232710 | Common:1; Rare:55 | ||||
chr11:117797149-117797481 | Common:3; Rare:106 | ||||
chr11:118790900-118791254 | Rare:102 | ||||
chr11:118997980-118998200 | Common:4; Rare:68 | ||||
chr11:119018292-119018452 | Common:6; Rare:65 | ||||
chr11:119057177-119057437 | Common:3; Rare:104 | ||||
chr11:119067730-119067826 | Rare:35 |