| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75992532-75992602 | Common:1; Rare:27 | ||||
| chr7:75994493-75994772 | Common:4; Rare:137 | ||||
| chr7:76047939-76048180 | Common:1; Rare:83 | ||||
| chr7:76302514-76303075 | Common:3; Rare:232; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):5 | ||||
| chr7:76358723-76358796 | Rare:19 | ||||
| chr7:76627248-76627358 | Common:5; Rare:31 | ||||
| chr7:77122265-77122688 | Common:2; Rare:87 | ||||
| chr7:77199693-77199845 | Rare:43 | ||||
| chr7:77199859-77200135 | Common:3; Rare:43 | ||||
| chr7:77696133-77696481 | Common:1; Rare:130 | ||||
| chr7:77696757-77696895 | Rare:61 | ||||
| chr7:77798344-77798910 | Common:1; Rare:137 | ||||
| chr7:79453560-79453721 | Rare:41 | ||||
| chr7:79453723-79454172 | Common:3; Rare:105 | ||||
| chr7:80134509-80134982 | Common:4; Rare:142 |