| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:46398541-46398616 | Common:1; Rare:11 | ||||
| chr10:47384219-47384696 | Common:4; Rare:122 | ||||
| chr10:47384710-47384765 | Rare:22 | ||||
| chr10:47384772-47384883 | Rare:44 | ||||
| chr10:47462310-47462370 | Rare:2 | ||||
| chr10:48306305-48306829 | Common:2; Rare:194 | ||||
| chr10:48306874-48307015 | Rare:44 | ||||
| chr10:48307031-48307184 | Common:2; Rare:42 | ||||
| chr10:48523698-48523834 | Common:1; Rare:31 | ||||
| chr10:48523920-48524095 | Rare:35 | ||||
| chr10:48656237-48656544 | Common:4; Rare:76 | ||||
| chr10:49538705-49538870 | Common:3; Rare:45 | ||||
| chr10:49538966-49539274 | Common:3; Rare:103; Clinvar:3; Clinvar (benign):3 | ||||
| chr10:49539447-49539493 | Rare:9 | ||||
| chr10:49539514-49539691 | Common:1; Rare:31 |