Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:118951829-118952166 | Common:1; Rare:95; Clinvar:7; Clinvar (benign):1 | ||||
chr8:119638808-119639070 | Common:1; Rare:42 | ||||
chr8:119832825-119832925 | Common:1; Rare:37 | ||||
chr8:120445088-120445461 | Common:1; Rare:97 | ||||
chr8:123042228-123042487 | Common:3; Rare:69 | ||||
chr8:123241291-123241444 | Common:1; Rare:69 | ||||
chr8:123416398-123416842 | Common:1; Rare:113 | ||||
chr8:124474935-124475112 | Rare:54 | ||||
chr8:124539026-124539198 | Common:2; Rare:97; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr8:125091699-125091915 | Common:2; Rare:75; Clinvar:1; Clinvar (benign):3 | ||||
chr8:127735890-127736099 | Rare:47 | ||||
chr8:127736118-127736269 | Common:3; Rare:30 | ||||
chr8:132675523-132675647 | Rare:40 | ||||
chr8:133571788-133572201 | Common:1; Rare:102 | ||||
chr8:134713020-134713149 | Common:1; Rare:44 |