| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:63521743-63522142 | Common:4; Rare:119 | ||||
| chr10:67837955-67838268 | Common:3; Rare:63 | ||||
| chr10:67884445-67884785 | Common:4; Rare:137 | ||||
| chr10:67884926-67885218 | Common:1; Rare:112 | ||||
| chr10:67885285-67885355 | Rare:24 | ||||
| chr10:68074222-68074287 | Rare:18 | ||||
| chr10:68074613-68074668 | Rare:13 | ||||
| chr10:68075024-68075144 | Common:1; Rare:22 | ||||
| chr10:68075171-68075527 | Common:4; Rare:142 | ||||
| chr10:68105968-68106051 | Rare:15 | ||||
| chr10:68231428-68231690 | Common:1; Rare:101; Clinvar (pathogenic):2 | ||||
| chr10:68331425-68332198 | Common:3; Rare:238 | ||||
| chr10:68332474-68332962 | Common:2; Rare:145 | ||||
| chr10:68406723-68407605 | Common:9; Rare:275 | ||||
| chr10:68471494-68471580 | Common:2; Rare:25 |