Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154172905-154173127 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr1:154183007-154183338 | Rare:107 | ||||
chr1:154212319-154212557 | Rare:93 | ||||
chr1:154219850-154220255 | Common:5; Rare:109 | ||||
chr1:154220341-154221036 | Common:1; Rare:231 | ||||
chr1:154221285-154221385 | Rare:21 | ||||
chr1:154254711-154254887 | Common:2; Rare:42 | ||||
chr1:154257114-154257434 | Rare:78 | ||||
chr1:154272420-154272775 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):3 | ||||
chr1:154627861-154628013 | Common:3; Rare:76 | ||||
chr1:154936594-154936812 | Common:3; Rare:72 | ||||
chr1:154968772-154969094 | Rare:75 | ||||
chr1:154970048-154970481 | Common:1; Rare:133 | ||||
chr1:154973716-154973928 | Rare:60 | ||||
chr1:154974265-154974745 | Rare:119 |