Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:100682446-100682613 | Common:1; Rare:75 | ||||
chr7:101137120-101137430 | Rare:76 | ||||
chr7:101223540-101223829 | Rare:98 | ||||
chr7:102822436-102822665 | Common:4; Rare:28 | ||||
chr7:105012680-105012823 | Common:1; Rare:51 | ||||
chr7:105013025-105013207 | Common:1; Rare:65 | ||||
chr7:106281600-106281846 | Rare:48 | ||||
chr7:112205565-112205679 | Rare:26 | ||||
chr7:113118526-113118671 | Common:1; Rare:51 | ||||
chr7:116211436-116211584 | Rare:30 | ||||
chr7:120780477-120780501 | Rare:3 | ||||
chr7:120780502-120780583 | Common:1; Rare:27 | ||||
chr7:122116630-122116888 | Rare:78; Clinvar (pathogenic):1 | ||||
chr7:128530414-128530590 | Rare:36 | ||||
chr7:130894195-130894432 | Common:5; Rare:52 |