| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:15860291-15860641 | Common:2; Rare:94 | ||||
| chr10:16436739-16437102 | Common:2; Rare:87 | ||||
| chr10:16817351-16817887 | Common:4; Rare:181 | ||||
| chr10:17201321-17201569 | Common:7; Rare:83 | ||||
| chr10:17201606-17201768 | Common:2; Rare:59 | ||||
| chr10:17227665-17228726 | Common:9; Rare:280 | ||||
| chr10:17230492-17230653 | Common:1; Rare:67 | ||||
| chr10:17454415-17454622 | Rare:48 | ||||
| chr10:17616684-17617110 | Common:6; Rare:206 | ||||
| chr10:17617296-17617676 | Common:5; Rare:132 | ||||
| chr10:17643853-17644295 | Common:2; Rare:137 | ||||
| chr10:18140139-18140396 | Common:3; Rare:59 | ||||
| chr10:18140646-18140815 | Common:2; Rare:62; Clinvar:3; Clinvar (benign):5 | ||||
| chr10:18651543-18651783 | Common:1; Rare:96 | ||||
| chr10:18659114-18659514 | Common:3; Rare:129 |