| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158802279-158802391 | Rare:32 | ||||
| chr3:160399171-160399307 | Rare:35; Clinvar:2 | ||||
| chr3:160399481-160399709 | Rare:68; Clinvar:2 | ||||
| chr3:160565414-160565845 | Common:2; Rare:155 | ||||
| chr3:167734839-167735254 | Common:5; Rare:130; Clinvar (benign):1 | ||||
| chr3:167735615-167735746 | Rare:32 | ||||
| chr3:168095898-168096224 | Common:1; Rare:110 | ||||
| chr3:169773299-169773424 | Rare:45 | ||||
| chr3:169812879-169813035 | Common:1; Rare:24 | ||||
| chr3:170870168-170870286 | Rare:63 | ||||
| chr3:179604621-179604852 | Common:2; Rare:85 | ||||
| chr3:180989650-180989796 | Rare:62; Clinvar:1 | ||||
| chr3:183884807-183885040 | Common:1; Rare:86 | ||||
| chr3:184135296-184135385 | Rare:25 | ||||
| chr3:184155254-184155448 | Rare:57 |