| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:45000192-45000541 | Common:2; Rare:91 | ||||
| chr10:45000766-45000964 | Common:1; Rare:85 | ||||
| chr10:45373942-45374262 | Common:3; Rare:107 | ||||
| chr10:45672784-45672905 | Common:1; Rare:41 | ||||
| chr10:45727083-45727307 | Common:4; Rare:81 | ||||
| chr10:45972349-45972564 | Common:1; Rare:70 | ||||
| chr10:48605072-48605213 | Common:1; Rare:42 | ||||
| chr10:49115443-49115641 | Rare:65 | ||||
| chr10:49539022-49539168 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:49941919-49942126 | Rare:62 | ||||
| chr10:50067822-50067995 | Common:4; Rare:78 | ||||
| chr10:50623359-50623520 | Common:2; Rare:31 | ||||
| chr10:50623887-50624094 | Common:1; Rare:80 | ||||
| chr10:50624852-50624976 | Common:1; Rare:47 | ||||
| chr10:51074364-51074566 | Common:1; Rare:45; Clinvar (benign):2 |