Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:227563340-227563650 | Common:2; Rare:85 | ||||
chr1:227563780-227563961 | Common:2; Rare:57 | ||||
chr1:227735231-227735520 | Common:4; Rare:160 | ||||
chr1:227947905-227948095 | Common:1; Rare:54 | ||||
chr1:228082469-228082756 | Common:3; Rare:117 | ||||
chr1:228103156-228103512 | Common:1; Rare:130 | ||||
chr1:228109246-228109481 | Rare:81 | ||||
chr1:228139834-228140094 | Common:1; Rare:62 | ||||
chr1:228140129-228140366 | Common:2; Rare:90 | ||||
chr1:228165370-228165800 | Rare:129; Clinvar (benign):1 | ||||
chr1:228165922-228166223 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):5 | ||||
chr1:228213631-228213856 | Common:1; Rare:64 | ||||
chr1:228407016-228407220 | Common:2; Rare:29 | ||||
chr1:228457473-228457638 | Rare:56 | ||||
chr1:228457817-228458116 | Common:2; Rare:123 |