Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:99971028-99971114 | Common:1; Rare:18 | ||||
chr7:99971148-99971334 | Rare:33 | ||||
chr7:99980515-99980766 | Common:3; Rare:43 | ||||
chr7:100335870-100336189 | Common:1; Rare:99 | ||||
chr7:100336303-100336371 | Common:1; Rare:24 | ||||
chr7:102822444-102822633 | Common:3; Rare:24 | ||||
chr7:105013031-105013199 | Rare:60 | ||||
chr7:105013574-105013627 | Rare:17 | ||||
chr7:105013628-105013657 | Rare:13 | ||||
chr7:107926313-107926393 | Common:1; Rare:32; Clinvar (benign):2 | ||||
chr7:107929063-107929329 | Common:2; Rare:74; Clinvar (benign):1 | ||||
chr7:107935643-107935909 | Common:2; Rare:43 | ||||
chr7:113118548-113118671 | Common:1; Rare:41 | ||||
chr7:116211444-116211617 | Rare:35 | ||||
chr7:129371673-129371929 | Rare:39 |