| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:47743655-47743810 | Rare:21 | ||||
| chr10:59175677-59175948 | Common:3; Rare:56 | ||||
| chr10:59626088-59626285 | Common:2; Rare:44 | ||||
| chr10:60573440-60573479 | Common:1; Rare:4 | ||||
| chr10:60573575-60573672 | Rare:18 | ||||
| chr10:68599750-68600056 | Common:1; Rare:51 | ||||
| chr10:68600170-68600353 | Rare:41 | ||||
| chr10:68600354-68600749 | Rare:67 | ||||
| chr10:71828859-71828898 | Common:1; Rare:15; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:71889110-71889220 | Common:1; Rare:20 | ||||
| chr10:72340850-72341138 | Common:3; Rare:90 | ||||
| chr10:73247176-73247341 | Rare:94 | ||||
| chr10:73730439-73730623 | Common:1; Rare:45 | ||||
| chr10:73999112-73999232 | Rare:24 | ||||
| chr10:74588689-74588759 | Rare:12 |