Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:178478512-178478721 | Common:1; Rare:71 | ||||
chr2:178480182-178480509 | Common:2; Rare:95 | ||||
chr2:179264501-179264848 | Common:3; Rare:130 | ||||
chr2:180007080-180007143 | Rare:11 | ||||
chr2:180980280-180980545 | Common:1; Rare:86 | ||||
chr2:182522500-182522677 | Common:2; Rare:35 | ||||
chr2:182522809-182522833 | Rare:4 | ||||
chr2:182715931-182716031 | Rare:21 | ||||
chr2:182716043-182716433 | Common:3; Rare:135 | ||||
chr2:183124190-183124483 | Common:4; Rare:92 | ||||
chr2:186485983-186486412 | Common:3; Rare:124 | ||||
chr2:186693898-186694132 | Rare:91 | ||||
chr2:186849071-186849266 | Common:4; Rare:60 | ||||
chr2:189441030-189441511 | Common:3; Rare:151 | ||||
chr2:189580759-189581135 | Common:3; Rare:113; Clinvar:1; Clinvar (benign):2 |