Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:113314408-113314602 | Rare:67 | ||||
chr11:113875472-113875762 | Common:4; Rare:103 | ||||
chr11:114059385-114059740 | Rare:79 | ||||
chr11:114295009-114295370 | Common:1; Rare:63 | ||||
chr11:114296256-114296908 | Common:1; Rare:142 | ||||
chr11:114298505-114298830 | Common:3; Rare:35 | ||||
chr11:114400444-114400784 | Common:2; Rare:132 | ||||
chr11:114440421-114440728 | Rare:72 | ||||
chr11:116772949-116773069 | Rare:46 | ||||
chr11:116829663-116830224 | Common:4; Rare:113 | ||||
chr11:116830404-116830893 | Common:5; Rare:164; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr11:116837343-116837691 | Common:2; Rare:83; Clinvar:3; Clinvar (benign):1 | ||||
chr11:117199018-117199430 | Common:6; Rare:130 | ||||
chr11:117232507-117232758 | Common:2; Rare:82 | ||||
chr11:117316249-117316413 | Common:1; Rare:35 |