| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:27179830-27180030 | Rare:79 | ||||
| chr7:27185180-27185433 | Common:1; Rare:90 | ||||
| chr7:27740061-27740216 | Common:5; Rare:45 | ||||
| chr7:28180437-28180677 | Common:1; Rare:77 | ||||
| chr7:28685949-28686149 | Rare:49 | ||||
| chr7:28958306-28958535 | Rare:63 | ||||
| chr7:30026625-30026928 | Rare:72 | ||||
| chr7:30478681-30478797 | Common:1; Rare:44 | ||||
| chr7:30504780-30505079 | Common:2; Rare:92 | ||||
| chr7:30594711-30594972 | Common:4; Rare:122; Clinvar:6; Clinvar (benign):7 | ||||
| chr7:30771226-30771494 | Common:1; Rare:80 | ||||
| chr7:30852102-30852447 | Common:1; Rare:75 | ||||
| chr7:32495240-32495575 | Rare:86 | ||||
| chr7:33109313-33109540 | Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:33129227-33129587 | Common:5; Rare:101 |