| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27100427-27100582 | Common:3; Rare:48; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:27154310-27154480 | Rare:45 | ||||
| chr10:27155212-27155460 | Common:7; Rare:110; Clinvar:2; Clinvar (benign):7 | ||||
| chr10:27743532-27743828 | Rare:66 | ||||
| chr10:27745399-27745649 | Rare:54 | ||||
| chr10:28238479-28238591 | Common:1; Rare:26 | ||||
| chr10:31319048-31319237 | Common:2; Rare:56 | ||||
| chr10:31928731-31928927 | Common:3; Rare:77 | ||||
| chr10:32056375-32056557 | Common:1; Rare:74 | ||||
| chr10:32446063-32446173 | Common:1; Rare:52 | ||||
| chr10:32958149-32958478 | Common:2; Rare:126 | ||||
| chr10:35090336-35090654 | Rare:98 | ||||
| chr10:35127016-35127169 | Common:1; Rare:52 | ||||
| chr10:42638499-42638582 | Common:1; Rare:40 | ||||
| chr10:43397194-43397413 | Common:1; Rare:68 |