Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:108559610-108559831 | Common:2; Rare:74 | ||||
chr6:108560726-108560972 | Rare:102 | ||||
chr6:108848325-108848482 | Rare:60 | ||||
chr6:109009396-109009689 | Common:2; Rare:86 | ||||
chr6:109094828-109095158 | Common:3; Rare:96 | ||||
chr6:109382372-109382806 | Common:5; Rare:146; Clinvar (benign):1 | ||||
chr6:109440567-109440927 | Common:2; Rare:120 | ||||
chr6:109455696-109456077 | Common:3; Rare:98 | ||||
chr6:109483148-109483242 | Rare:42 | ||||
chr6:109691151-109691322 | Common:3; Rare:43; Clinvar:4; Clinvar (benign):3 | ||||
chr6:110179941-110180154 | Common:2; Rare:62 | ||||
chr6:110874633-110874798 | Common:4; Rare:54 | ||||
chr6:110958453-110958775 | Common:7; Rare:100 | ||||
chr6:110981877-110982118 | Common:3; Rare:114 | ||||
chr6:111483139-111483544 | Common:1; Rare:142 |