| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:24980089-24980414 | Common:8; Rare:135 | ||||
| chr7:25125217-25125448 | Rare:103; Clinvar:3 | ||||
| chr7:26177812-26178045 | Common:1; Rare:73 | ||||
| chr7:26196366-26196515 | Common:1; Rare:65; Clinvar (benign):2 | ||||
| chr7:26196555-26197036 | Common:2; Rare:170; Clinvar (benign):3 | ||||
| chr7:26201367-26201555 | Rare:71 | ||||
| chr7:26201568-26201826 | Common:2; Rare:135 | ||||
| chr7:26202078-26202450 | Rare:163 | ||||
| chr7:27740063-27740231 | Common:5; Rare:48 | ||||
| chr7:28180576-28180823 | Common:1; Rare:68 | ||||
| chr7:28685990-28686196 | Rare:52 | ||||
| chr7:29989646-29989947 | Rare:116 | ||||
| chr7:30028254-30028422 | Common:1; Rare:54 | ||||
| chr7:30504571-30504654 | Rare:32 | ||||
| chr7:30504696-30505081 | Common:4; Rare:129 |