| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:14878606-14878891 | Common:2; Rare:91 | ||||
| chr10:14954062-14954220 | Rare:43 | ||||
| chr10:16817373-16817722 | Common:3; Rare:124 | ||||
| chr10:17228463-17228675 | Common:1; Rare:57 | ||||
| chr10:17643866-17644188 | Common:1; Rare:97 | ||||
| chr10:22316196-22316453 | Common:2; Rare:113 | ||||
| chr10:24466435-24466511 | Rare:11 | ||||
| chr10:27154323-27154508 | Rare:53 | ||||
| chr10:27155227-27155421 | Common:6; Rare:87; Clinvar:2; Clinvar (benign):6 | ||||
| chr10:32056398-32056523 | Common:1; Rare:54 | ||||
| chr10:32958149-32958472 | Common:2; Rare:124 | ||||
| chr10:42638520-42638606 | Common:1; Rare:40 | ||||
| chr10:42782756-42782830 | Rare:22 | ||||
| chr10:43407751-43407999 | Common:3; Rare:85 | ||||
| chr10:43409125-43409426 | Common:3; Rare:105 |