| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:726616-726734 | Rare:46 | ||||
| chr7:727210-727411 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:727568-727834 | Rare:46 | ||||
| chr7:768177-768702 | Common:11; Rare:165 | ||||
| chr7:816418-816669 | Common:2; Rare:90 | ||||
| chr7:975450-975680 | Common:1; Rare:101 | ||||
| chr7:1028260-1028526 | Common:2; Rare:102 | ||||
| chr7:1028792-1029053 | Common:3; Rare:31 | ||||
| chr7:1138034-1138093 | Rare:24 | ||||
| chr7:1138192-1138448 | Common:2; Rare:80 | ||||
| chr7:1459277-1459790 | Common:2; Rare:181 | ||||
| chr7:1504286-1504455 | Common:1; Rare:76 | ||||
| chr7:1537280-1537514 | Rare:78 | ||||
| chr7:1538064-1538293 | Common:1; Rare:77 | ||||
| chr7:1569962-1570170 | Common:1; Rare:70 |