| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:56639432-56639517 | Rare:10 | ||||
| chr3:57015628-57015638 | Rare:1 | ||||
| chr3:57577075-57577407 | Common:2; Rare:62 | ||||
| chr3:57580432-57580486 | Rare:9 | ||||
| chr3:57647765-57647998 | Common:1; Rare:37 | ||||
| chr3:57882523-57882747 | Rare:32 | ||||
| chr3:57883653-57883873 | Rare:36 | ||||
| chr3:58009143-58009276 | Rare:31 | ||||
| chr3:58010516-58010546 | Rare:5 | ||||
| chr3:58085812-58085980 | Common:2; Rare:29 | ||||
| chr3:58091519-58091776 | Common:1; Rare:33 | ||||
| chr3:58094831-58095217 | Common:2; Rare:78; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:58095604-58095868 | Common:3; Rare:40 | ||||
| chr3:58100229-58100564 | Common:4; Rare:52 | ||||
| chr3:58103989-58104192 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |