| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:57952294-57952543 | Rare:38 | ||||
| chr3:58010608-58010624 | Rare:1 | ||||
| chr3:58012659-58012857 | Rare:30 | ||||
| chr3:58034155-58034386 | Common:2; Rare:29 | ||||
| chr3:58035260-58035470 | Rare:30 | ||||
| chr3:58048308-58048582 | Common:1; Rare:52 | ||||
| chr3:58049274-58049494 | Common:1; Rare:32 | ||||
| chr3:58082733-58082742 | Rare:2 | ||||
| chr3:58085838-58086164 | Common:3; Rare:56 | ||||
| chr3:58090103-58090196 | Common:1; Rare:16 | ||||
| chr3:58091109-58091434 | Rare:35 | ||||
| chr3:58091441-58091776 | Common:1; Rare:42 | ||||
| chr3:58103932-58104217 | Common:4; Rare:85; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:58105041-58105447 | Common:3; Rare:101; Clinvar:3; Clinvar (benign):2 | ||||
| chr3:58108412-58108650 | Common:1; Rare:66; Clinvar:4; Clinvar (pathogenic):1 |