| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:30594943-30595127 | Common:3; Rare:79; Clinvar:5; Clinvar (benign):8 | ||||
| chr7:32495293-32495557 | Rare:62 | ||||
| chr7:35694548-35694726 | Common:1; Rare:36 | ||||
| chr7:35694892-35695254 | Common:4; Rare:102 | ||||
| chr7:35800939-35801255 | Common:2; Rare:133 | ||||
| chr7:40134581-40134706 | Rare:44 | ||||
| chr7:42932151-42932392 | Rare:91 | ||||
| chr7:44116178-44116504 | Rare:85 | ||||
| chr7:44582217-44582441 | Common:1; Rare:71 | ||||
| chr7:44796395-44796694 | Common:2; Rare:107 | ||||
| chr7:44848168-44848471 | Common:2; Rare:76 | ||||
| chr7:44999603-44999756 | Common:3; Rare:57 | ||||
| chr7:45111677-45111815 | Common:1; Rare:49 | ||||
| chr7:48089012-48089307 | Common:5; Rare:81 | ||||
| chr7:56051378-56051851 | Common:1; Rare:176; Clinvar:5; Clinvar (benign):1 |