| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:63268850-63269018 | Common:1; Rare:36 | ||||
| chr10:63269031-63269388 | Common:2; Rare:72 | ||||
| chr10:63465965-63466146 | Common:1; Rare:85 | ||||
| chr10:63521194-63521525 | Common:7; Rare:117 | ||||
| chr10:63521743-63522082 | Common:4; Rare:111 | ||||
| chr10:67838020-67838243 | Common:3; Rare:47 | ||||
| chr10:67885106-67885235 | Common:1; Rare:49 | ||||
| chr10:68075189-68075484 | Common:4; Rare:125 | ||||
| chr10:68231487-68231669 | Rare:71; Clinvar (pathogenic):2 | ||||
| chr10:68331601-68331702 | Rare:21 | ||||
| chr10:68331838-68332152 | Common:2; Rare:125 | ||||
| chr10:68332877-68333016 | Common:1; Rare:35 | ||||
| chr10:68407185-68407442 | Common:5; Rare:88 | ||||
| chr10:68471701-68472033 | Common:2; Rare:138; Clinvar:1; Clinvar (benign):3 | ||||
| chr10:68721000-68721566 | Common:5; Rare:179 |