Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:227735181-227735498 | Common:9; Rare:338 | ||||
chr1:227947926-227948083 | Common:1; Rare:42 | ||||
chr1:228082445-228082804 | Common:8; Rare:267 | ||||
chr1:228103203-228103509 | Common:2; Rare:206 | ||||
chr1:228109197-228109502 | Rare:186 | ||||
chr1:228139922-228140379 | Common:6; Rare:289 | ||||
chr1:228165409-228165810 | Rare:208; Clinvar (benign):4 | ||||
chr1:228165880-228166260 | Common:4; Rare:289; Clinvar:8; Clinvar (benign):14; Clinvar (pathogenic):10 | ||||
chr1:228213132-228213446 | Common:3; Rare:82 | ||||
chr1:228406765-228407207 | Common:11; Rare:181 | ||||
chr1:228457734-228458194 | Common:3; Rare:361 | ||||
chr1:228487020-228487470 | Common:9; Rare:248 | ||||
chr1:228735130-228735520 | Common:2; Rare:178 | ||||
chr1:229271011-229271301 | Rare:190 | ||||
chr1:229342479-229342706 | Rare:145 |