| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76302786-76303075 | Rare:128; Clinvar:11; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
| chr7:77696221-77696471 | Rare:100 | ||||
| chr7:77798387-77798969 | Common:1; Rare:139 | ||||
| chr7:79453560-79454089 | Common:3; Rare:131 | ||||
| chr7:80134618-80134928 | Common:3; Rare:104 | ||||
| chr7:80918975-80919293 | Common:3; Rare:100 | ||||
| chr7:83162808-83163018 | Rare:75 | ||||
| chr7:84194624-84194919 | Common:3; Rare:37 | ||||
| chr7:84194920-84195171 | Common:5; Rare:57 | ||||
| chr7:87152300-87152468 | Common:1; Rare:52 | ||||
| chr7:87345412-87345736 | Common:5; Rare:96 | ||||
| chr7:87876329-87876702 | Common:3; Rare:163 | ||||
| chr7:90346564-90346736 | Common:3; Rare:72 | ||||
| chr7:91880668-91880820 | Common:1; Rare:41 | ||||
| chr7:91940735-91940964 | Common:3; Rare:67; Clinvar:2 |