Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:177264630-177264865 | Common:2; Rare:76 | ||||
chr2:177392655-177392823 | Common:1; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
chr2:177552764-177552828 | Rare:23 | ||||
chr2:178072696-178072825 | Rare:32 | ||||
chr2:178451083-178451418 | Common:6; Rare:100; Clinvar:4; Clinvar (benign):3 | ||||
chr2:178478534-178478686 | Common:1; Rare:48 | ||||
chr2:179264502-179264848 | Common:3; Rare:130 | ||||
chr2:180980258-180980545 | Common:1; Rare:90 | ||||
chr2:181891605-181892354 | Common:6; Rare:305 | ||||
chr2:182716204-182716399 | Rare:62 | ||||
chr2:183078685-183078792 | Rare:19 | ||||
chr2:186485978-186486364 | Common:3; Rare:111 | ||||
chr2:188291772-188292014 | Common:3; Rare:73 | ||||
chr2:188292716-188292869 | Common:1; Rare:40 | ||||
chr2:188292969-188293054 | Rare:9 |