Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:238203549-238203773 | Common:4; Rare:82 | ||||
chr2:239401641-239401750 | Rare:52 | ||||
chr2:240025276-240025477 | Common:2; Rare:79; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr2:240560760-240560873 | Common:1; Rare:49 | ||||
chr2:241048161-241048427 | Rare:64 | ||||
chr2:241051126-241051464 | Common:3; Rare:65 | ||||
chr2:241102263-241102357 | Common:2; Rare:39 | ||||
chr2:241149455-241149621 | Common:2; Rare:51 | ||||
chr2:241239752-241240014 | Rare:83 | ||||
chr2:241272794-241273016 | Rare:79 | ||||
chr2:241315109-241315398 | Common:5; Rare:98 | ||||
chr2:241315644-241315994 | Common:5; Rare:136 | ||||
chr2:241508551-241508901 | Common:1; Rare:114 | ||||
chr2:241637527-241637704 | Common:1; Rare:96 | ||||
chr2:241686792-241686970 | Rare:52 |