Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:120719601-120719832 | Rare:46 | ||||
chr3:130111470-130111771 | Common:3; Rare:73 | ||||
chr3:130112416-130112547 | Common:2; Rare:33 | ||||
chr3:131361648-131361916 | Common:3; Rare:80 | ||||
chr3:133491107-133491322 | Rare:44 | ||||
chr3:149285889-149285970 | Common:1; Rare:17 | ||||
chr3:150408860-150409014 | Rare:45 | ||||
chr3:152270034-152270075 | Rare:11 | ||||
chr3:155704908-155705076 | Rare:15 | ||||
chr3:156816986-156817239 | Rare:79 | ||||
chr3:157174857-157175255 | Common:3; Rare:174 | ||||
chr3:158698207-158698515 | Common:3; Rare:55 | ||||
chr3:158713810-158714042 | Common:2; Rare:50 | ||||
chr3:169764853-169764861 | Rare:4; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr3:170356734-170356752 | Rare:7 |