Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:172711038-172711368 | Common:1; Rare:89 | ||||
chr3:172750356-172750794 | Common:4; Rare:99 | ||||
chr3:172750909-172751017 | Rare:33 | ||||
chr3:177196387-177196550 | Rare:43 | ||||
chr3:179147988-179148118 | Rare:30 | ||||
chr3:179347595-179347774 | Common:1; Rare:41 | ||||
chr3:179562632-179563034 | Rare:134 | ||||
chr3:179604581-179604848 | Common:3; Rare:105 | ||||
chr3:180601975-180602242 | Common:1; Rare:84 | ||||
chr3:180989606-180989823 | Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
chr3:183162662-183162871 | Common:5; Rare:43 | ||||
chr3:183253852-183254168 | Common:2; Rare:95 | ||||
chr3:183635539-183635713 | Common:2; Rare:53 | ||||
chr3:184017876-184018073 | Common:1; Rare:58 | ||||
chr3:184135219-184135394 | Common:2; Rare:53; Clinvar:5 |