Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69088007-69088226 | Rare:49 | ||||
chr10:69801624-69801953 | Common:2; Rare:83 | ||||
chr10:70132807-70132882 | Rare:17 | ||||
chr10:70170414-70170680 | Common:4; Rare:90 | ||||
chr10:70233342-70233566 | Common:5; Rare:80 | ||||
chr10:70403970-70404173 | Rare:77 | ||||
chr10:70815830-70815999 | Rare:66 | ||||
chr10:70887867-70887970 | Common:1; Rare:22 | ||||
chr10:70888529-70888609 | Common:1; Rare:27; Clinvar:3; Clinvar (benign):1 | ||||
chr10:71819549-71819804 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):2 | ||||
chr10:72626035-72626272 | Common:1; Rare:58 | ||||
chr10:73096751-73097035 | Common:4; Rare:83 | ||||
chr10:73167941-73168133 | Rare:51 | ||||
chr10:73252387-73252801 | Common:3; Rare:128; Clinvar:5; Clinvar (benign):4 | ||||
chr10:73495606-73495763 | Rare:31 |