| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:63133075-63133406 | Common:4; Rare:199 | ||||
| chr10:63464840-63465400 | Common:3; Rare:169 | ||||
| chr10:63465960-63466140 | Common:1; Rare:127 | ||||
| chr10:63521073-63521521 | Common:15; Rare:252 | ||||
| chr10:63521789-63521976 | Common:8; Rare:137 | ||||
| chr10:67838024-67838243 | Common:3; Rare:47 | ||||
| chr10:67884485-67884731 | Common:5; Rare:174 | ||||
| chr10:67884760-67885500 | Common:5; Rare:367 | ||||
| chr10:68075079-68075469 | Common:8; Rare:257 | ||||
| chr10:68331510-68331750 | Rare:49 | ||||
| chr10:68331880-68332155 | Common:4; Rare:212 | ||||
| chr10:68332888-68333028 | Common:1; Rare:33 | ||||
| chr10:68407166-68407440 | Common:9; Rare:159 | ||||
| chr10:68471885-68472033 | Common:2; Rare:154; Clinvar (benign):2 | ||||
| chr10:68527272-68527651 | Common:5; Rare:198; Clinvar (pathogenic):1 |