Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:81761504-81761553 | Common:3; Rare:11; Clinvar (benign):1 | ||||
chr3:98952825-98952974 | Common:1; Rare:27 | ||||
chr3:98966962-98967112 | Rare:26 | ||||
chr3:98980988-98981086 | Rare:23 | ||||
chr3:101576981-101577264 | Common:2; Rare:70 | ||||
chr3:104440032-104440323 | Common:1; Rare:72 | ||||
chr3:104445430-104445729 | Common:5; Rare:76 | ||||
chr3:107240581-107240759 | Rare:78 | ||||
chr3:129794971-129795211 | Common:1; Rare:49 | ||||
chr3:150408860-150409002 | Rare:41 | ||||
chr3:159732274-159732390 | Common:1; Rare:19 | ||||
chr3:169765053-169765197 | Rare:66; Clinvar (pathogenic):2 | ||||
chr3:183447456-183447680 | Common:1; Rare:55 | ||||
chr3:192887844-192887895 | Common:2; Rare:10 | ||||
chr3:194583909-194584026 | Common:4; Rare:39 |