Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:208266040-208266302 | Common:9; Rare:93; Clinvar:1; Clinvar (benign):2 | ||||
chr2:210225079-210225185 | Rare:27 | ||||
chr2:210225311-210225470 | Rare:27 | ||||
chr2:215311879-215312160 | Common:8; Rare:113 | ||||
chr2:215436051-215436284 | Common:2; Rare:78 | ||||
chr2:216081743-216081906 | Common:1; Rare:53 | ||||
chr2:216498753-216498886 | Common:3; Rare:56 | ||||
chr2:217978817-217978877 | Rare:14 | ||||
chr2:218217076-218217246 | Common:1; Rare:60 | ||||
chr2:218270054-218270533 | Common:5; Rare:148; Clinvar:2; Clinvar (benign):1 | ||||
chr2:218289992-218290034 | Rare:6 | ||||
chr2:218292477-218292626 | Common:1; Rare:43 | ||||
chr2:218568301-218568629 | Common:2; Rare:88 | ||||
chr2:218568781-218568850 | Rare:12 | ||||
chr2:218659339-218659362 | Rare:8 |