| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:23438734-23439200 | Common:7; Rare:178 | ||||
| chr10:23439327-23439468 | Common:1; Rare:47 | ||||
| chr10:24208768-24208967 | Common:1; Rare:58 | ||||
| chr10:24209498-24209588 | Rare:17 | ||||
| chr10:24722905-24723308 | Common:3; Rare:101 | ||||
| chr10:24952268-24952373 | Rare:18 | ||||
| chr10:24952456-24952704 | Common:2; Rare:72 | ||||
| chr10:25016581-25016764 | Common:4; Rare:85 | ||||
| chr10:25016946-25017144 | Common:4; Rare:84 | ||||
| chr10:26437683-26437801 | Rare:20 | ||||
| chr10:26438014-26438433 | Common:2; Rare:99 | ||||
| chr10:26438607-26438856 | Common:4; Rare:61 | ||||
| chr10:26697137-26697746 | Common:4; Rare:154; Clinvar (benign):1 | ||||
| chr10:26860467-26860709 | Common:3; Rare:46 | ||||
| chr10:26860813-26861055 | Common:2; Rare:86 |