Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:87227031-87227404 | Common:2; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
chr3:88058186-88058509 | Common:1; Rare:80 | ||||
chr3:88058875-88059322 | Common:4; Rare:174 | ||||
chr3:88149645-88149782 | Rare:32 | ||||
chr3:88149840-88150285 | Common:6; Rare:160 | ||||
chr3:89107550-89107782 | Common:1; Rare:65 | ||||
chr3:93979935-93980244 | Common:4; Rare:119; Clinvar:1; Clinvar (benign):2 | ||||
chr3:94062880-94063101 | Rare:55 | ||||
chr3:97764485-97764833 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
chr3:98901637-98901951 | Rare:111 | ||||
chr3:99817562-99818008 | Rare:133 | ||||
chr3:99876128-99876257 | Rare:32 | ||||
chr3:100260691-100261061 | Rare:109 | ||||
chr3:100334676-100334758 | Common:1; Rare:37 | ||||
chr3:100401095-100401215 | Rare:33 |