Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:71819463-71819902 | Common:1; Rare:173; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851181-71851464 | Common:5; Rare:120; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216215-72216559 | Common:3; Rare:98 | ||||
chr10:72273662-72273988 | Rare:97 | ||||
chr10:72354883-72355023 | Common:2; Rare:69 | ||||
chr10:73110357-73110536 | Rare:38 | ||||
chr10:73167958-73168127 | Rare:38 | ||||
chr10:73252594-73252808 | Rare:59; Clinvar:4 | ||||
chr10:73495565-73495766 | Rare:39 | ||||
chr10:73495810-73496130 | Common:2; Rare:89 | ||||
chr10:73625983-73626121 | Rare:26 | ||||
chr10:73744002-73744436 | Common:1; Rare:110 | ||||
chr10:73781969-73782084 | Common:1; Rare:36 | ||||
chr10:73800436-73800733 | Common:3; Rare:75 | ||||
chr10:73874492-73874718 | Rare:52 |