Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:186567293-186567426 | Common:3; Rare:33 | ||||
chr3:186806432-186806782 | Rare:95 | ||||
chr3:186930411-186930823 | Common:2; Rare:97 | ||||
chr3:188153777-188153880 | Common:1; Rare:19 | ||||
chr3:193593123-193593192 | Rare:20 | ||||
chr3:195543191-195543456 | Common:3; Rare:96 | ||||
chr3:195583909-195584203 | Common:9; Rare:64 | ||||
chr3:196287621-196287813 | Common:1; Rare:62 | ||||
chr3:196568530-196568647 | Common:2; Rare:29 | ||||
chr3:196867748-196867935 | Rare:60 | ||||
chr3:196942375-196942686 | Common:1; Rare:131 | ||||
chr3:197736841-197737193 | Common:3; Rare:117 | ||||
chr3:197749672-197749979 | Common:1; Rare:105 | ||||
chr3:197949890-197950240 | Common:4; Rare:107; Clinvar (benign):2 | ||||
chr3:197959969-197960254 | Common:1; Rare:99 |