| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:13988758-13989006 | Common:1; Rare:58 | ||||
| chr7:13989056-13989350 | Common:4; Rare:71 | ||||
| chr7:14902625-14902635 | Rare:3 | ||||
| chr7:14902963-14903273 | Rare:64 | ||||
| chr7:16465730-16465947 | Rare:37 | ||||
| chr7:16645629-16646237 | Common:5; Rare:212 | ||||
| chr7:16753632-16753930 | Common:2; Rare:104 | ||||
| chr7:17940399-17940595 | Common:2; Rare:93 | ||||
| chr7:18495346-18495789 | Rare:102 | ||||
| chr7:20330896-20331077 | Common:2; Rare:46 | ||||
| chr7:20331728-20331834 | Common:1; Rare:36 | ||||
| chr7:22500169-22500249 | Rare:33 | ||||
| chr7:22822715-22822954 | Common:3; Rare:89 | ||||
| chr7:23105661-23105890 | Common:4; Rare:117; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:23106593-23106672 | Rare:13 |