Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:216081771-216081914 | Common:1; Rare:52 | ||||
chr2:216498740-216498896 | Common:6; Rare:67 | ||||
chr2:218216812-218217226 | Common:2; Rare:116 | ||||
chr2:218270091-218270602 | Common:5; Rare:165; Clinvar:6; Clinvar (benign):2 | ||||
chr2:218287270-218287366 | Rare:15 | ||||
chr2:218568290-218568635 | Common:3; Rare:91 | ||||
chr2:218568781-218568956 | Common:1; Rare:55 | ||||
chr2:218659334-218659363 | Rare:9 | ||||
chr2:218659605-218659755 | Rare:39 | ||||
chr2:218671974-218672339 | Common:2; Rare:90 | ||||
chr2:219176883-219177119 | Common:4; Rare:71 | ||||
chr2:219206683-219206923 | Rare:87 | ||||
chr2:219217756-219218029 | Common:1; Rare:61; Clinvar:2 | ||||
chr2:219229330-219229422 | Rare:29 | ||||
chr2:219229559-219229912 | Common:2; Rare:110 |