| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:35695061-35695251 | Common:1; Rare:66 | ||||
| chr7:35800944-35801255 | Common:2; Rare:131 | ||||
| chr7:37916811-37916971 | Rare:42 | ||||
| chr7:40134403-40134558 | Rare:67 | ||||
| chr7:40134583-40134842 | Rare:72 | ||||
| chr7:41700572-41700679 | Rare:17 | ||||
| chr7:42932160-42932407 | Rare:101 | ||||
| chr7:43926378-43926475 | Rare:30 | ||||
| chr7:44573859-44574062 | Common:3; Rare:65 | ||||
| chr7:44582199-44582529 | Common:1; Rare:123 | ||||
| chr7:44606456-44606635 | Common:1; Rare:61 | ||||
| chr7:45921174-45921282 | Rare:51 | ||||
| chr7:55365285-55365350 | Rare:19 | ||||
| chr7:56051420-56051837 | Common:1; Rare:157; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:66682065-66682195 | Common:6; Rare:53 |