| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:84459215-84459606 | Common:3; Rare:100; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905469-84906146 | Common:3; Rare:190 | ||||
| chr2:84906983-84907243 | Common:1; Rare:48 | ||||
| chr2:84970670-84970750 | Common:1; Rare:22 | ||||
| chr2:85327902-85328094 | Common:3; Rare:89 | ||||
| chr2:85328273-85328405 | Common:1; Rare:24 | ||||
| chr2:85354427-85354790 | Common:1; Rare:122 | ||||
| chr2:85539072-85539353 | Common:3; Rare:143; Clinvar (benign):7 | ||||
| chr2:85539971-85540117 | Rare:38 | ||||
| chr2:85561424-85561581 | Rare:58; Clinvar:4 | ||||
| chr2:85584302-85584466 | Common:1; Rare:47 | ||||
| chr2:85595555-85595847 | Common:2; Rare:102 | ||||
| chr2:85602629-85602904 | Rare:72 | ||||
| chr2:85611750-85612113 | Rare:172 | ||||
| chr2:85753573-85753874 | Common:2; Rare:87 |