| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:65755463-65755523 | Common:1; Rare:22 | ||||
| chr7:65770719-65770922 | Common:6; Rare:64 | ||||
| chr7:66493507-66493742 | Common:4; Rare:98 | ||||
| chr7:66592308-66592702 | Common:3; Rare:112 | ||||
| chr7:66654461-66654568 | Rare:40 | ||||
| chr7:66844878-66845131 | Common:2; Rare:102 | ||||
| chr7:67302402-67302710 | Common:5; Rare:100 | ||||
| chr7:67302879-67302910 | Rare:9 | ||||
| chr7:70693791-70694082 | Common:2; Rare:92 | ||||
| chr7:73005809-73006140 | Rare:38 | ||||
| chr7:73734802-73735115 | Common:2; Rare:69 | ||||
| chr7:73739647-73739787 | Common:7; Rare:26 | ||||
| chr7:73769457-73769707 | Common:2; Rare:89 | ||||
| chr7:74038263-74038484 | Rare:35 | ||||
| chr7:74051551-74051776 | Rare:51; Clinvar (pathogenic):1 |