| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:15209850-15210090 | Common:1; Rare:48 | ||||
| chr10:15247758-15248201 | Common:4; Rare:107 | ||||
| chr10:15325751-15325856 | Rare:20 | ||||
| chr10:16828274-16828391 | Common:1; Rare:15 | ||||
| chr10:16891210-16891550 | Common:5; Rare:67 | ||||
| chr10:16891611-16892208 | Common:17; Rare:263 | ||||
| chr10:17029651-17029790 | Rare:25 | ||||
| chr10:17062920-17063490 | Common:1; Rare:112 | ||||
| chr10:17064507-17064619 | Rare:26 | ||||
| chr10:17100540-17100900 | Common:1; Rare:61 | ||||
| chr10:17115490-17116000 | Common:5; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:17215021-17215325 | Common:2; Rare:57 | ||||
| chr10:17216345-17216496 | Rare:26 | ||||
| chr10:17273400-17273950 | Common:11; Rare:121 | ||||
| chr10:17348419-17348819 | Common:12; Rare:142 |