| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:53748750-53749131 | Rare:78 | ||||
| chr3:53768626-53768837 | Common:1; Rare:25 | ||||
| chr3:53768860-53768960 | Common:1; Rare:25 | ||||
| chr3:53774035-53774314 | Common:2; Rare:40 | ||||
| chr3:53845647-53845886 | Rare:62 | ||||
| chr3:56783939-56784179 | Rare:44 | ||||
| chr3:56917705-56917960 | Rare:37 | ||||
| chr3:56918306-56918375 | Rare:12 | ||||
| chr3:57228463-57228600 | Rare:25 | ||||
| chr3:57557241-57557386 | Rare:52 | ||||
| chr3:57557418-57557579 | Rare:49 | ||||
| chr3:57671412-57671715 | Common:2; Rare:47 | ||||
| chr3:57983839-57984123 | Common:1; Rare:42 | ||||
| chr3:58111739-58111875 | Common:1; Rare:27; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:58116206-58116426 | Common:2; Rare:48 |