| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:1047855-1048317 | Common:2; Rare:180 | ||||
| chr10:1048710-1049160 | Common:15; Rare:902 | ||||
| chr10:1049115-1049830 | Common:51; Rare:1047 | ||||
| chr10:1056110-1056470 | Common:2; Rare:154 | ||||
| chr10:1056490-1057000 | Common:29; Rare:689 | ||||
| chr10:3066323-3066723 | Common:6; Rare:101 | ||||
| chr10:3066832-3067754 | Common:16; Rare:595 | ||||
| chr10:3067829-3068788 | Common:10; Rare:392 | ||||
| chr10:3068961-3070358 | Common:30; Rare:717 | ||||
| chr10:3172130-3172500 | Common:7; Rare:175 | ||||
| chr10:3172677-3173511 | Common:16; Rare:276 | ||||
| chr10:3781849-3782249 | Common:2; Rare:106; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr10:3785150-3785678 | Common:25; Rare:1004 | ||||
| chr10:4825860-4826295 | Common:20; Rare:273 | ||||
| chr10:4826310-4826870 | Common:29; Rare:357 |