| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:197498750-197499051 | Common:5; Rare:84; Clinvar (benign):4 | ||||
| chr2:202376105-202376324 | Rare:99 | ||||
| chr2:206084358-206084615 | Common:1; Rare:56 | ||||
| chr2:207163479-207163703 | Common:1; Rare:36 | ||||
| chr2:218277366-218277729 | Rare:101 | ||||
| chr2:236988754-236989111 | Common:3; Rare:78 | ||||
| chr2:237156562-237156828 | Common:4; Rare:50 | ||||
| chr2:237333448-237333751 | Common:1; Rare:66; Clinvar:5 | ||||
| chr2:241053780-241054075 | Rare:61 | ||||
| chr20:2624222-2624493 | Common:1; Rare:60 | ||||
| chr20:2821415-2821572 | Common:2; Rare:30 | ||||
| chr20:3307165-3307230 | Common:1; Rare:12 | ||||
| chr20:3712534-3712753 | Common:1; Rare:40 | ||||
| chr20:3784365-3784390 | Rare:3 | ||||
| chr20:4822531-4822800 | Common:5; Rare:58 |