| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:75985353-75985944 | Common:8; Rare:231; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr7:75994473-75994779 | Common:4; Rare:148 | ||||
| chr7:76047950-76048206 | Common:2; Rare:87 | ||||
| chr7:76303007-76303075 | Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:76303841-76304050 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr7:76625666-76625985 | Common:5; Rare:89 | ||||
| chr7:77122281-77122642 | Common:2; Rare:74 | ||||
| chr7:77199646-77199861 | Common:1; Rare:61 | ||||
| chr7:77696195-77696613 | Common:2; Rare:179 | ||||
| chr7:77696830-77697012 | Rare:78 | ||||
| chr7:77798353-77798910 | Common:1; Rare:136 | ||||
| chr7:79453615-79454089 | Common:3; Rare:116 | ||||
| chr7:80919035-80919352 | Common:3; Rare:114 | ||||
| chr7:83162566-83162991 | Common:2; Rare:117 | ||||
| chr7:87152164-87152802 | Common:3; Rare:183 |