| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50328090-50328490 | Common:2; Rare:389 | ||||
| chr3:50336916-50337316 | Common:2; Rare:115 | ||||
| chr3:50337241-50338207 | Common:8; Rare:500 | ||||
| chr3:50338124-50338616 | Common:5; Rare:325 | ||||
| chr3:50340143-50340543 | Common:2; Rare:84 | ||||
| chr3:50340774-50341538 | Common:11; Rare:445; Clinvar (benign):1 | ||||
| chr3:50350696-50351443 | Common:19; Rare:445 | ||||
| chr3:50359410-50359848 | Common:12; Rare:438 | ||||
| chr3:50365067-50365467 | Common:6; Rare:663; Clinvar:22; Clinvar (benign):7 | ||||
| chr3:50503594-50504027 | Common:2; Rare:234 | ||||
| chr3:50567620-50568020 | Common:1; Rare:372 | ||||
| chr3:50568560-50568960 | Common:2; Rare:66 | ||||
| chr3:50568938-50569648 | Common:10; Rare:698 | ||||
| chr3:50577488-50577648 | Common:2; Rare:45 | ||||
| chr3:50610726-50611560 | Common:2; Rare:183 |