| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:180989629-180989790 | Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:181711736-181711924 | Rare:68 | ||||
| chr3:183253133-183253292 | Common:2; Rare:48 | ||||
| chr3:183555632-183555954 | Common:1; Rare:62 | ||||
| chr3:183635487-183635713 | Common:3; Rare:71 | ||||
| chr3:184135248-184135403 | Common:2; Rare:43; Clinvar:2 | ||||
| chr3:184249532-184249678 | Rare:39 | ||||
| chr3:184298948-184299283 | Common:3; Rare:104 | ||||
| chr3:184335863-184335937 | Rare:23 | ||||
| chr3:184711614-184711726 | Common:2; Rare:29 | ||||
| chr3:184711926-184712292 | Common:2; Rare:122 | ||||
| chr3:185254029-185254252 | Common:1; Rare:60 | ||||
| chr3:185282838-185283014 | Common:1; Rare:47 | ||||
| chr3:185498933-185499149 | Rare:81 | ||||
| chr3:185823185-185823350 | Rare:51 |