| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:69451337-69451581 | Common:4; Rare:118 | ||||
| chr10:70132736-70132920 | Rare:98 | ||||
| chr10:70146169-70146314 | Common:4; Rare:94 | ||||
| chr10:70146563-70146939 | Common:2; Rare:183 | ||||
| chr10:70170428-70170758 | Common:7; Rare:197 | ||||
| chr10:70233300-70233603 | Common:11; Rare:205; Clinvar (benign):1 | ||||
| chr10:70382583-70382783 | Common:9; Rare:132 | ||||
| chr10:70403971-70404218 | Rare:175 | ||||
| chr10:70888534-70888666 | Common:3; Rare:76; Clinvar:9; Clinvar (benign):3 | ||||
| chr10:71212526-71212761 | Common:1; Rare:69 | ||||
| chr10:71319136-71319313 | Common:4; Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:71773508-71773746 | Common:3; Rare:67 | ||||
| chr10:71827870-71828381 | Common:2; Rare:235; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr10:71851181-71851441 | Common:10; Rare:220; Clinvar:8; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr10:72215590-72216180 | Common:1; Rare:165 |