| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:71319156-71319348 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:71319603-71319805 | Common:2; Rare:47 | ||||
| chr10:71396829-71396933 | Common:2; Rare:18 | ||||
| chr10:71773443-71773762 | Common:4; Rare:98 | ||||
| chr10:71773846-71773990 | Rare:25 | ||||
| chr10:71850741-71850891 | Rare:36 | ||||
| chr10:71850966-71851131 | Rare:63 | ||||
| chr10:71851161-71851564 | Common:5; Rare:143; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr10:71964074-71964363 | Common:1; Rare:78 | ||||
| chr10:71964451-71964538 | Common:4; Rare:25; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:71964757-71965023 | Common:2; Rare:59 | ||||
| chr10:72215837-72216146 | Rare:108 | ||||
| chr10:72216207-72216428 | Rare:82 | ||||
| chr10:72273350-72274120 | Common:2; Rare:190 | ||||
| chr10:72274368-72274407 | Rare:13 |