| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:76302314-76302759 | Common:4; Rare:155; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr7:76302762-76303075 | Rare:131; Clinvar:11; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
| chr7:76303639-76303865 | Common:1; Rare:101; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr7:76627251-76627361 | Common:5; Rare:29 | ||||
| chr7:77122114-77122230 | Common:1; Rare:22 | ||||
| chr7:77122266-77122698 | Common:2; Rare:90 | ||||
| chr7:77199701-77199909 | Rare:54 | ||||
| chr7:77415569-77415783 | Common:1; Rare:51 | ||||
| chr7:77416293-77416644 | Common:5; Rare:94 | ||||
| chr7:77536841-77537160 | Common:4; Rare:96 | ||||
| chr7:77537416-77537567 | Rare:56 | ||||
| chr7:77696116-77696543 | Common:1; Rare:171 | ||||
| chr7:77696792-77697010 | Rare:98 | ||||
| chr7:77697021-77697165 | Common:1; Rare:49 | ||||
| chr7:77798344-77798980 | Common:1; Rare:150 |