Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:119294570-119294699 | Rare:25; Clinvar:1; Clinvar (benign):1 | ||||
chr3:119463585-119463817 | Common:5; Rare:71 | ||||
chr3:119468826-119469015 | Rare:69 | ||||
chr3:119498412-119498723 | Common:4; Rare:99 | ||||
chr3:119498792-119498885 | Rare:32 | ||||
chr3:119676900-119677231 | Common:17; Rare:117 | ||||
chr3:119677318-119677519 | Common:1; Rare:72 | ||||
chr3:120093491-120093764 | Rare:69 | ||||
chr3:120094436-120094781 | Common:3; Rare:108 | ||||
chr3:120349276-120349430 | Common:2; Rare:50 | ||||
chr3:120450865-120451352 | Rare:150 | ||||
chr3:120742503-120742777 | Common:2; Rare:77 | ||||
chr3:121749137-121749279 | Rare:25 | ||||
chr3:121834966-121835238 | Common:3; Rare:86; Clinvar:6; Clinvar (benign):2 | ||||
chr3:122383192-122383312 | Common:1; Rare:39 |