Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:75672069-75672267 | Common:19; Rare:8 | ||||
chr3:75672521-75672708 | Rare:1 | ||||
chr3:80770367-80770706 | Common:9; Rare:87 | ||||
chr3:81761498-81761614 | Common:5; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
chr3:86793823-86794066 | Common:1; Rare:44 | ||||
chr3:98980987-98981082 | Rare:22 | ||||
chr3:98981106-98981194 | Rare:12 | ||||
chr3:101576982-101577049 | Rare:16 | ||||
chr3:101676254-101676500 | Common:2; Rare:83 | ||||
chr3:107240610-107240737 | Rare:55 | ||||
chr3:112640342-112640484 | Common:1; Rare:25 | ||||
chr3:120095037-120095249 | Rare:60 | ||||
chr3:129021166-129021221 | Rare:7 | ||||
chr3:130112414-130112547 | Common:2; Rare:33 | ||||
chr3:150408859-150409012 | Rare:45 |