| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:43915666-43915796 | Common:1; Rare:20 | ||||
| chr20:43915968-43916090 | Rare:20 | ||||
| chr20:44210327-44210428 | Rare:33 | ||||
| chr20:44210502-44211147 | Common:6; Rare:214 | ||||
| chr20:44311069-44311286 | Common:1; Rare:89 | ||||
| chr20:44475740-44476015 | Common:1; Rare:107 | ||||
| chr20:44521643-44521741 | Common:1; Rare:27 | ||||
| chr20:44521957-44522270 | Common:3; Rare:92 | ||||
| chr20:44582441-44582598 | Rare:25 | ||||
| chr20:44651155-44651255 | Common:1; Rare:25 | ||||
| chr20:44651635-44652057 | Common:1; Rare:110; Clinvar (benign):1 | ||||
| chr20:44885258-44885300 | Rare:12 | ||||
| chr20:44885368-44885798 | Common:8; Rare:140 | ||||
| chr20:44885925-44886157 | Rare:83 | ||||
| chr20:44909860-44910184 | Common:2; Rare:133 |