Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:112025293-112025629 | Common:4; Rare:101; Clinvar:1; Clinvar (benign):7 | ||||
chr11:112073985-112074356 | Common:1; Rare:79 | ||||
chr11:112086720-112086913 | Rare:82; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr11:112226314-112226711 | Common:1; Rare:159; Clinvar:1; Clinvar (pathogenic):3 | ||||
chr11:112961214-112961661 | Common:5; Rare:197 | ||||
chr11:113314448-113314602 | Rare:54 | ||||
chr11:113875497-113875809 | Common:4; Rare:119 | ||||
chr11:114059417-114059734 | Rare:67 | ||||
chr11:114400446-114400753 | Common:2; Rare:123 | ||||
chr11:115504320-115504636 | Common:2; Rare:107 | ||||
chr11:116772932-116773031 | Rare:42 | ||||
chr11:117144183-117144418 | Common:2; Rare:106 | ||||
chr11:117232034-117232191 | Rare:41 | ||||
chr11:117232515-117232760 | Common:2; Rare:83 | ||||
chr11:117316051-117316413 | Common:1; Rare:90 |