| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:27155156-27155453 | Common:7; Rare:121; Clinvar:5; Clinvar (benign):7 | ||||
| chr10:28532454-28532927 | Common:5; Rare:173 | ||||
| chr10:28533002-28533188 | Rare:72 | ||||
| chr10:31928729-31928892 | Common:3; Rare:66 | ||||
| chr10:32056372-32056584 | Common:2; Rare:83 | ||||
| chr10:32378724-32378854 | Rare:20 | ||||
| chr10:32446031-32446239 | Common:1; Rare:97 | ||||
| chr10:32958149-32958522 | Common:2; Rare:140 | ||||
| chr10:35126665-35127007 | Common:3; Rare:107 | ||||
| chr10:37857600-37857737 | Common:2; Rare:51 | ||||
| chr10:38010530-38010762 | Common:2; Rare:110 | ||||
| chr10:42782684-42782830 | Rare:38 | ||||
| chr10:43138374-43138519 | Common:2; Rare:53 | ||||
| chr10:43396632-43396939 | Common:1; Rare:102 | ||||
| chr10:43397188-43397474 | Common:1; Rare:90 |