| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:47781646-47781713 | Rare:20 | ||||
| chr3:47824913-47825125 | Rare:58 | ||||
| chr3:48089246-48089347 | Rare:32 | ||||
| chr3:48301325-48301449 | Common:1; Rare:39 | ||||
| chr3:48301485-48301597 | Common:1; Rare:40 | ||||
| chr3:48440027-48440317 | Common:1; Rare:110 | ||||
| chr3:48446589-48446743 | Rare:54 | ||||
| chr3:48504090-48504297 | Common:2; Rare:68 | ||||
| chr3:48567708-48567861 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr3:48584116-48584192 | Common:2; Rare:12 | ||||
| chr3:48847671-48847947 | Common:1; Rare:74 | ||||
| chr3:48918805-48918985 | Common:2; Rare:99 | ||||
| chr3:48982960-48983204 | Rare:54 | ||||
| chr3:49007359-49007503 | Rare:62 | ||||
| chr3:49018552-49018592 | Rare:16 |