Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:168179818-168180359 | Common:10; Rare:132 | ||||
chr1:168387130-168387470 | Common:2; Rare:63 | ||||
chr1:168880100-168880609 | Common:2; Rare:135 | ||||
chr1:168906483-168906655 | Rare:27 | ||||
chr1:168907073-168907552 | Common:10; Rare:196 | ||||
chr1:169003852-169005083 | Common:18; Rare:383 | ||||
chr1:169031730-169031897 | Rare:27 | ||||
chr1:169107097-169107243 | Common:1; Rare:27 | ||||
chr1:169109662-169110115 | Common:12; Rare:180 | ||||
chr1:169485235-169485342 | Rare:27 | ||||
chr1:169507526-169507667 | Rare:26 | ||||
chr1:169529000-169529670 | Common:11; Rare:206; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
chr1:169865000-169865701 | Common:4; Rare:158 | ||||
chr1:169868925-169869883 | Common:5; Rare:269 | ||||
chr1:170174414-170174814 | Common:11; Rare:159 |