| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100041428-100041695 | Rare:33 | ||||
| chr3:100042243-100042471 | Rare:46 | ||||
| chr3:100060642-100060725 | Common:1; Rare:13 | ||||
| chr3:100275358-100275583 | Common:1; Rare:38 | ||||
| chr3:100732976-100733112 | Common:1; Rare:24 | ||||
| chr3:100744714-100744966 | Common:3; Rare:61; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:100748115-100748169 | Rare:14 | ||||
| chr3:100775114-100775298 | Common:2; Rare:51 | ||||
| chr3:100775321-100775488 | Rare:29 | ||||
| chr3:100780171-100780237 | Rare:19 | ||||
| chr3:100791864-100792149 | Rare:50 | ||||
| chr3:100797861-100797897 | Common:1; Rare:7 | ||||
| chr3:100838214-100838466 | Rare:54 | ||||
| chr3:100839567-100839659 | Common:1; Rare:18 | ||||
| chr3:100955005-100955124 | Rare:8 |