Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:68233009-68233129 | Rare:27 | ||||
chr1:68497025-68497358 | Common:3; Rare:105 | ||||
chr1:70205480-70205770 | Rare:107 | ||||
chr1:70221271-70221531 | Rare:114 | ||||
chr1:70354647-70354852 | Rare:69 | ||||
chr1:70410983-70411303 | Common:3; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
chr1:70411412-70411834 | Common:2; Rare:139 | ||||
chr1:71080984-71081398 | Rare:116 | ||||
chr1:72282830-72283330 | Common:7; Rare:166 | ||||
chr1:74198054-74198346 | Common:3; Rare:142 | ||||
chr1:74733005-74733369 | Common:6; Rare:130 | ||||
chr1:75724210-75724410 | Common:3; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
chr1:75724623-75724838 | Common:2; Rare:98; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:75786039-75786314 | Common:4; Rare:116 | ||||
chr1:76074539-76074760 | Common:2; Rare:87 |