| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:975513-975674 | Common:1; Rare:64 | ||||
| chr7:1028278-1028474 | Rare:78 | ||||
| chr7:1086559-1086872 | Common:1; Rare:81 | ||||
| chr7:1086968-1087192 | Common:1; Rare:79 | ||||
| chr7:1138197-1138424 | Common:2; Rare:70 | ||||
| chr7:1570007-1570110 | Common:1; Rare:30 | ||||
| chr7:2232897-2233022 | Rare:52 | ||||
| chr7:2242168-2242274 | Common:2; Rare:61 | ||||
| chr7:2354041-2354105 | Rare:31 | ||||
| chr7:2555485-2555839 | Common:5; Rare:97 | ||||
| chr7:2645446-2645551 | Rare:20 | ||||
| chr7:4775498-4775652 | Common:6; Rare:61; Clinvar:1 | ||||
| chr7:5513746-5513876 | Common:1; Rare:55 | ||||
| chr7:6009029-6009349 | Common:4; Rare:136; Clinvar:3; Clinvar (benign):15 | ||||
| chr7:6104622-6105002 | Common:5; Rare:135 |