Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32107968-32108118 | Rare:57 | ||||
chr1:32179581-32179765 | Rare:40 | ||||
chr1:32200578-32200680 | Rare:23 | ||||
chr1:32205494-32205693 | Common:1; Rare:78 | ||||
chr1:32222323-32222543 | Rare:89 | ||||
chr1:32251155-32251328 | Common:1; Rare:46 | ||||
chr1:32291821-32292156 | Common:1; Rare:96 | ||||
chr1:32330563-32330877 | Rare:62 | ||||
chr1:32351377-32351639 | Common:1; Rare:68 | ||||
chr1:32394410-32394663 | Common:1; Rare:68 | ||||
chr1:32650918-32651318 | Common:2; Rare:150 | ||||
chr1:32817240-32817826 | Common:1; Rare:156; Clinvar:5; Clinvar (benign):4 | ||||
chr1:32818177-32818286 | Rare:33 | ||||
chr1:33021402-33021655 | Rare:58; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:33036806-33037155 | Rare:125; Clinvar (pathogenic):1 |