Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:144170557-144170880 | Common:2; Rare:105 | ||||
chr5:145835296-145835499 | Common:2; Rare:48 | ||||
chr5:145937633-145937791 | Rare:39 | ||||
chr5:146182497-146182866 | Common:4; Rare:106 | ||||
chr5:147234931-147235090 | Rare:50 | ||||
chr5:148383854-148384022 | Rare:52 | ||||
chr5:149141428-149141789 | Common:1; Rare:94 | ||||
chr5:149345401-149345615 | Common:1; Rare:88 | ||||
chr5:149551334-149551649 | Rare:75 | ||||
chr5:149960575-149960925 | Rare:117; Clinvar:7 | ||||
chr5:150357431-150357749 | Rare:104; Clinvar:2; Clinvar (benign):4 | ||||
chr5:150449662-150449795 | Common:4; Rare:46 | ||||
chr5:150700975-150701156 | Common:2; Rare:75 | ||||
chr5:150758566-150758869 | Common:2; Rare:94 | ||||
chr5:150904738-150904999 | Common:2; Rare:62 |