Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70170425-70170686 | Common:4; Rare:87 | ||||
chr10:71773431-71773752 | Common:4; Rare:96 | ||||
chr10:71819140-71819356 | Rare:43 | ||||
chr10:71851183-71851486 | Common:5; Rare:121; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr10:72273665-72274132 | Common:1; Rare:130 | ||||
chr10:73167948-73168138 | Rare:48 | ||||
chr10:73495595-73495763 | Rare:35 | ||||
chr10:73743891-73744085 | Common:1; Rare:50 | ||||
chr10:73744288-73744419 | Rare:26 | ||||
chr10:73781945-73782071 | Common:1; Rare:36 | ||||
chr10:73997908-73998193 | Common:1; Rare:83 | ||||
chr10:80079031-80079282 | Common:2; Rare:104 | ||||
chr10:80205480-80205646 | Common:2; Rare:63 | ||||
chr10:84139286-84139586 | Common:3; Rare:79 | ||||
chr10:87094879-87095231 | Common:1; Rare:81; Clinvar:2 |