| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50450716-50450817 | Rare:33 | ||||
| chr3:51627276-51627613 | Common:1; Rare:63 | ||||
| chr3:53156528-53156653 | Common:2; Rare:31 | ||||
| chr3:53185673-53186025 | Rare:97; Clinvar:3 | ||||
| chr3:53787520-53787632 | Common:1; Rare:17 | ||||
| chr3:57245905-57246215 | Rare:54 | ||||
| chr3:57267488-57267792 | Rare:62 | ||||
| chr3:57268126-57268430 | Rare:46 | ||||
| chr3:57577304-57577597 | Common:1; Rare:70 | ||||
| chr3:64010257-64010261 | Rare:1 | ||||
| chr3:64568451-64568657 | Common:2; Rare:50 | ||||
| chr3:64684761-64684980 | Rare:31 | ||||
| chr3:64685181-64685259 | Rare:14 | ||||
| chr3:66384211-66384372 | Common:2; Rare:71; Clinvar (benign):1 | ||||
| chr3:66394081-66394396 | Common:2; Rare:76; Clinvar (benign):1 |