Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:100401378-100401580 | Common:1; Rare:45 | ||||
chr3:101686662-101686844 | Common:2; Rare:80 | ||||
chr3:111859513-111859819 | Rare:94 | ||||
chr3:112561607-112561702 | Rare:34 | ||||
chr3:112561872-112562088 | Common:1; Rare:66 | ||||
chr3:112640952-112641209 | Common:3; Rare:73 | ||||
chr3:113211363-113211565 | Common:2; Rare:47 | ||||
chr3:113746184-113746300 | Rare:53 | ||||
chr3:114056475-114056782 | Common:2; Rare:121 | ||||
chr3:119498345-119498625 | Common:4; Rare:94 | ||||
chr3:120742507-120742782 | Common:2; Rare:76 | ||||
chr3:121749643-121750012 | Common:1; Rare:85 | ||||
chr3:121834987-121835210 | Common:3; Rare:74; Clinvar:6; Clinvar (benign):2 | ||||
chr3:122383211-122383283 | Common:1; Rare:23 | ||||
chr3:122416049-122416229 | Rare:57 |