Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:188152945-188153038 | Common:1; Rare:16 | ||||
chr3:188153761-188154010 | Common:1; Rare:44 | ||||
chr3:188154060-188154232 | Rare:58 | ||||
chr3:188947534-188947606 | Rare:9 | ||||
chr3:189100131-189100173 | Rare:9 | ||||
chr3:189631183-189631471 | Common:3; Rare:58; Clinvar (benign):1 | ||||
chr3:191329331-191329613 | Common:3; Rare:79 | ||||
chr3:193240987-193241324 | Common:4; Rare:115 | ||||
chr3:193593101-193593404 | Rare:93; Clinvar:2; Clinvar (benign):2 | ||||
chr3:194672153-194672471 | Common:1; Rare:96 | ||||
chr3:195542904-195542933 | Rare:10 | ||||
chr3:195542936-195543095 | Common:1; Rare:60 | ||||
chr3:195543104-195543483 | Common:4; Rare:124 | ||||
chr3:195583878-195584144 | Rare:53 | ||||
chr3:196287606-196287823 | Common:1; Rare:68 |