| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50299272-50299692 | Common:1; Rare:100 | ||||
| chr3:50303532-50303595 | Common:1; Rare:10 | ||||
| chr3:50312373-50312470 | Rare:30 | ||||
| chr3:50328173-50328353 | Rare:53 | ||||
| chr3:50350697-50350905 | Common:1; Rare:31 | ||||
| chr3:50359379-50359597 | Common:3; Rare:61 | ||||
| chr3:50365106-50365382 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:50567635-50567898 | Rare:82 | ||||
| chr3:50569460-50569499 | Rare:7 | ||||
| chr3:50611636-50611889 | Rare:59 | ||||
| chr3:51384996-51385403 | Common:2; Rare:125 | ||||
| chr3:51499941-51500331 | Common:1; Rare:79 | ||||
| chr3:51670984-51671288 | Common:2; Rare:90 | ||||
| chr3:51941978-51942287 | Common:2; Rare:68 | ||||
| chr3:51975048-51975138 | Common:1; Rare:33 |