Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:56467527-56467699 | Common:2; Rare:72; Clinvar (benign):5 | ||||
chr4:56977574-56977785 | Common:1; Rare:81 | ||||
chr4:57110014-57110286 | Rare:94 | ||||
chr4:67545423-67545748 | Common:2; Rare:84 | ||||
chr4:67701051-67701419 | Common:4; Rare:168 | ||||
chr4:68349971-68350213 | Common:1; Rare:86 | ||||
chr4:69050987-69051288 | Rare:68 | ||||
chr4:70688454-70688607 | Common:2; Rare:46 | ||||
chr4:70902191-70902413 | Common:4; Rare:80 | ||||
chr4:70993487-70993822 | Common:5; Rare:100 | ||||
chr4:73069675-73069865 | Common:1; Rare:90 | ||||
chr4:73258526-73258883 | Common:1; Rare:99 | ||||
chr4:73259124-73259180 | Rare:10 | ||||
chr4:73620365-73620657 | Common:2; Rare:80 | ||||
chr4:73869759-73869922 | Common:1; Rare:67 |