| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68407179-68407357 | Common:4; Rare:57 | ||||
| chr10:68721091-68721281 | Common:2; Rare:62 | ||||
| chr10:68900988-68901374 | Common:3; Rare:153 | ||||
| chr10:68988558-68988904 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:69087982-69088236 | Rare:53 | ||||
| chr10:70170414-70170680 | Common:4; Rare:90 | ||||
| chr10:70888529-70888612 | Common:1; Rare:28; Clinvar:3; Clinvar (benign):1 | ||||
| chr10:71773462-71773751 | Common:3; Rare:87 | ||||
| chr10:71819463-71819836 | Common:1; Rare:142; Clinvar:5; Clinvar (benign):2 | ||||
| chr10:71851183-71851389 | Common:5; Rare:95; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr10:72088694-72088755 | Rare:10 | ||||
| chr10:72216232-72216630 | Common:3; Rare:104 | ||||
| chr10:72273682-72273939 | Rare:68 | ||||
| chr10:72354893-72355005 | Common:1; Rare:59 | ||||
| chr10:73096804-73097028 | Common:3; Rare:69 |