| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:727252-727304 | Rare:14; Clinvar:1 | ||||
| chr7:975513-975660 | Common:1; Rare:62 | ||||
| chr7:1028296-1028465 | Rare:65 | ||||
| chr7:1055293-1055372 | Rare:33 | ||||
| chr7:1088098-1088206 | Rare:32 | ||||
| chr7:1537318-1537490 | Rare:58 | ||||
| chr7:1538074-1538289 | Common:1; Rare:70 | ||||
| chr7:1570018-1570188 | Common:1; Rare:52 | ||||
| chr7:2242171-2242268 | Common:2; Rare:57 | ||||
| chr7:2403296-2403622 | Common:1; Rare:128 | ||||
| chr7:4775510-4775691 | Common:4; Rare:84; Clinvar:1 | ||||
| chr7:4882214-4882324 | Rare:23 | ||||
| chr7:5423540-5423629 | Rare:20 | ||||
| chr7:5513746-5513906 | Common:2; Rare:71 | ||||
| chr7:5529446-5529810 | Common:1; Rare:159; Clinvar:1; Clinvar (benign):8 |