Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161209479-161210101 | Common:1; Rare:260; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
chr1:161225570-161226210 | Common:62; Rare:445 | ||||
chr1:161226266-161227777 | Common:9; Rare:998 | ||||
chr1:161305629-161306069 | Common:6; Rare:220; Clinvar:16; Clinvar (benign):6 | ||||
chr1:161306051-161307059 | Common:11; Rare:957; Clinvar:47; Clinvar (benign):27; Clinvar (pathogenic):33 | ||||
chr1:161307350-161307730 | Rare:196; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):9 | ||||
chr1:161314060-161314570 | Common:26; Rare:603; Clinvar:60; Clinvar (benign):35; Clinvar (pathogenic):6 | ||||
chr1:161314812-161314957 | Rare:66 | ||||
chr1:161505186-161505543 | Common:6; Rare:291 | ||||
chr1:161505468-161505977 | Common:1; Rare:154 | ||||
chr1:161505912-161507048 | Common:11; Rare:684; Clinvar (benign):6 | ||||
chr1:161523798-161524246 | Common:22; Rare:375 | ||||
chr1:161524254-161524654 | Common:10; Rare:192 | ||||
chr1:161706480-161707004 | Common:5; Rare:181 | ||||
chr1:161706995-161707403 | Common:9; Rare:226 |