Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:102736876-102736921 | Common:1; Rare:11 | ||||
chr2:105337508-105337602 | Rare:42 | ||||
chr2:108534203-108534502 | Common:7; Rare:123 | ||||
chr2:108719414-108719577 | Common:2; Rare:67; Clinvar (benign):2 | ||||
chr2:109613879-109614065 | Common:2; Rare:64 | ||||
chr2:111884151-111884255 | Rare:30 | ||||
chr2:112255032-112255187 | Common:2; Rare:70 | ||||
chr2:112645707-112645947 | Common:1; Rare:89 | ||||
chr2:113627055-113627303 | Common:3; Rare:73 | ||||
chr2:113756556-113756759 | Common:2; Rare:67 | ||||
chr2:113889962-113890165 | Common:2; Rare:70 | ||||
chr2:119366795-119367080 | Common:1; Rare:86 | ||||
chr2:119679072-119679216 | Common:3; Rare:46 | ||||
chr2:120252630-120252967 | Common:3; Rare:110 | ||||
chr2:121530574-121530884 | Common:7; Rare:131 |