Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:184249463-184249771 | Common:1; Rare:91 | ||||
chr3:184362813-184362902 | Rare:14 | ||||
chr3:184712033-184712268 | Common:1; Rare:79 | ||||
chr3:185282855-185283014 | Common:1; Rare:40 | ||||
chr3:185498968-185499149 | Rare:64 | ||||
chr3:185824953-185825320 | Rare:103 | ||||
chr3:186567293-186567434 | Common:3; Rare:36 | ||||
chr3:187291684-187291864 | Common:1; Rare:65 | ||||
chr3:187291914-187292141 | Common:16; Rare:60 | ||||
chr3:188153709-188153938 | Common:1; Rare:42 | ||||
chr3:188154091-188154227 | Rare:44 | ||||
chr3:191329093-191329425 | Common:2; Rare:90 | ||||
chr3:193593100-193593376 | Rare:91; Clinvar:2; Clinvar (benign):2 | ||||
chr3:194486994-194487146 | Common:3; Rare:68 | ||||
chr3:195271104-195271228 | Rare:49 |