Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:94706127-94706327 | Common:2; Rare:46 | ||||
chr7:97972261-97972365 | Rare:26 | ||||
chr7:100335862-100336158 | Common:1; Rare:98 | ||||
chr7:100336327-100336369 | Common:1; Rare:16 | ||||
chr7:100345782-100346095 | Common:4; Rare:37 | ||||
chr7:104940794-104940944 | Rare:45 | ||||
chr7:105012684-105012816 | Rare:46 | ||||
chr7:105013025-105013212 | Common:1; Rare:66 | ||||
chr7:105013581-105013657 | Rare:30 | ||||
chr7:105106927-105107217 | Common:2; Rare:69 | ||||
chr7:105111580-105111875 | Rare:69 | ||||
chr7:107926345-107926397 | Common:1; Rare:19; Clinvar (benign):1 | ||||
chr7:107986028-107986190 | Rare:38 | ||||
chr7:108004372-108004596 | Common:1; Rare:37 | ||||
chr7:128530542-128530590 | Rare:10 |