Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:48569632-48569823 | Common:1; Rare:55 | ||||
chr3:53818941-53819165 | Common:3; Rare:55 | ||||
chr3:57920002-57920141 | Rare:25 | ||||
chr3:66382369-66382589 | Common:5; Rare:88 | ||||
chr3:73520940-73521263 | Rare:52 | ||||
chr3:75435068-75435386 | Common:4; Rare:110 | ||||
chr3:80770411-80770529 | Common:1; Rare:5 | ||||
chr3:81761510-81761599 | Common:5; Rare:27; Clinvar (benign):1 | ||||
chr3:101576981-101577099 | Rare:33 | ||||
chr3:101676310-101676506 | Rare:64 | ||||
chr3:106644234-106644473 | Common:5; Rare:58 | ||||
chr3:107240600-107240808 | Rare:78 | ||||
chr3:118810795-118810903 | Rare:48 | ||||
chr3:123638926-123639021 | Rare:12 | ||||
chr3:124032453-124032504 | Rare:9 |