| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50359344-50359630 | Common:3; Rare:78 | ||||
| chr3:50365106-50365376 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:50569460-50569499 | Rare:7 | ||||
| chr3:50611754-50611892 | Rare:31 | ||||
| chr3:50617412-50617506 | Rare:9 | ||||
| chr3:51385019-51385336 | Common:1; Rare:90 | ||||
| chr3:51941985-51942291 | Common:2; Rare:68 | ||||
| chr3:51942704-51943303 | Common:3; Rare:95 | ||||
| chr3:51944271-51944555 | Common:2; Rare:95 | ||||
| chr3:51975013-51975129 | Common:1; Rare:40 | ||||
| chr3:51983113-51983565 | Common:2; Rare:101 | ||||
| chr3:51988732-51988936 | Rare:63; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:51995424-51995633 | Common:2; Rare:58 | ||||
| chr3:51995848-51996042 | Common:2; Rare:71 | ||||
| chr3:52239075-52239257 | Common:2; Rare:66 |