Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:57597321-57597661 | Common:4; Rare:106 | ||||
chr3:58491816-58492114 | Common:3; Rare:78 | ||||
chr3:62318890-62319079 | Rare:78 | ||||
chr3:63863777-63864150 | Common:7; Rare:123 | ||||
chr3:64013595-64013782 | Common:2; Rare:58 | ||||
chr3:67654513-67654770 | Common:2; Rare:109 | ||||
chr3:69080358-69080477 | Rare:48 | ||||
chr3:77039995-77040131 | Rare:36 | ||||
chr3:87227201-87227334 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
chr3:88058903-88059320 | Common:3; Rare:163 | ||||
chr3:88149877-88149999 | Rare:37 | ||||
chr3:94062920-94063052 | Rare:34 | ||||
chr3:97764474-97764566 | Rare:17 | ||||
chr3:98732279-98732327 | Rare:9 | ||||
chr3:98732350-98732950 | Rare:125 |