| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:62268610-62269110 | Common:4; Rare:262 | ||||
| chr10:62804415-62804807 | Common:8; Rare:201 | ||||
| chr10:63133072-63133407 | Common:2; Rare:103 | ||||
| chr10:63521073-63521499 | Common:15; Rare:246 | ||||
| chr10:63521759-63522185 | Common:8; Rare:223 | ||||
| chr10:67838020-67838269 | Common:5; Rare:86 | ||||
| chr10:67884439-67884734 | Common:7; Rare:220 | ||||
| chr10:67884780-67885347 | Common:6; Rare:351 | ||||
| chr10:68074607-68074999 | Common:4; Rare:159 | ||||
| chr10:68075073-68075512 | Common:8; Rare:277 | ||||
| chr10:68105923-68106289 | Common:2; Rare:112 | ||||
| chr10:68108832-68109700 | Common:9; Rare:275; Clinvar (benign):1 | ||||
| chr10:68231428-68231810 | Common:2; Rare:204; Clinvar (pathogenic):4 | ||||
| chr10:68331590-68331728 | Rare:28 | ||||
| chr10:68331842-68332240 | Common:5; Rare:256 |