| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17809183-17809533 | Rare:53 | ||||
| chr10:18651543-18651748 | Common:1; Rare:86 | ||||
| chr10:18659103-18659406 | Common:3; Rare:91 | ||||
| chr10:19816264-19816653 | Common:6; Rare:84 | ||||
| chr10:21173765-21174036 | Common:4; Rare:73; Clinvar (benign):1 | ||||
| chr10:22316292-22316510 | Common:1; Rare:94 | ||||
| chr10:22321303-22321505 | Rare:69 | ||||
| chr10:22321506-22321590 | Rare:32 | ||||
| chr10:23343969-23343978 | Rare:2 | ||||
| chr10:23343992-23344088 | Common:1; Rare:26 | ||||
| chr10:23344636-23344700 | Rare:11 | ||||
| chr10:23344728-23345137 | Common:4; Rare:101 | ||||
| chr10:24722704-24722823 | Rare:31 | ||||
| chr10:25016310-25016608 | Common:7; Rare:86 | ||||
| chr10:26438065-26438419 | Common:2; Rare:84 |