| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76303717-76303852 | Common:1; Rare:60; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chr7:77122312-77122659 | Common:2; Rare:70 | ||||
| chr7:77199792-77199867 | Rare:21 | ||||
| chr7:77696232-77696544 | Rare:139 | ||||
| chr7:77696757-77696989 | Rare:105 | ||||
| chr7:77798344-77798927 | Common:1; Rare:142 | ||||
| chr7:79453609-79453753 | Common:1; Rare:38 | ||||
| chr7:79453799-79454117 | Common:2; Rare:74 | ||||
| chr7:80134531-80134935 | Common:4; Rare:127 | ||||
| chr7:80918979-80919277 | Common:3; Rare:93 | ||||
| chr7:87152307-87152655 | Common:2; Rare:105 | ||||
| chr7:87219640-87219883 | Rare:66 | ||||
| chr7:87345437-87345749 | Common:6; Rare:96 | ||||
| chr7:87876224-87876652 | Common:2; Rare:183 | ||||
| chr7:88306857-88307150 | Rare:63 |