Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69416905-69417068 | Common:3; Rare:48 | ||||
chr10:70170414-70170742 | Common:4; Rare:104 | ||||
chr10:70233356-70233552 | Common:4; Rare:68 | ||||
chr10:71773508-71773746 | Common:3; Rare:67 | ||||
chr10:71819514-71819897 | Common:1; Rare:158; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71851199-71851464 | Common:5; Rare:111; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72216232-72216523 | Common:3; Rare:89 | ||||
chr10:72273662-72273942 | Rare:72 | ||||
chr10:72354883-72355023 | Common:2; Rare:69 | ||||
chr10:73110379-73110522 | Rare:28 | ||||
chr10:73167965-73168142 | Rare:43 | ||||
chr10:73252594-73252789 | Rare:52; Clinvar:4 | ||||
chr10:73495600-73495764 | Rare:32 | ||||
chr10:73625962-73626109 | Rare:26 | ||||
chr10:73651038-73651262 | Common:2; Rare:45 |