| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76302877-76303076 | Rare:84; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr7:76358738-76359084 | Common:1; Rare:128 | ||||
| chr7:77696221-77696465 | Rare:96 | ||||
| chr7:77798393-77798971 | Common:1; Rare:138 | ||||
| chr7:79453559-79453686 | Rare:32 | ||||
| chr7:79453776-79454123 | Common:2; Rare:85 | ||||
| chr7:80134611-80134935 | Common:3; Rare:107 | ||||
| chr7:80918979-80919348 | Common:3; Rare:125 | ||||
| chr7:81770038-81770354 | Rare:64; Clinvar:1 | ||||
| chr7:84194922-84195226 | Common:6; Rare:61 | ||||
| chr7:85186716-85186963 | Common:3; Rare:50 | ||||
| chr7:87152255-87152480 | Common:1; Rare:78 | ||||
| chr7:87345407-87345739 | Common:5; Rare:97 | ||||
| chr7:87876204-87876649 | Common:2; Rare:187 | ||||
| chr7:88209914-88210015 | Rare:30 |