| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645721-16646217 | Common:4; Rare:175 | ||||
| chr7:17298454-17298659 | Common:3; Rare:49 | ||||
| chr7:17940429-17940574 | Common:1; Rare:71 | ||||
| chr7:20331714-20331834 | Common:1; Rare:40 | ||||
| chr7:22500136-22500238 | Common:1; Rare:39 | ||||
| chr7:22822704-22822969 | Common:3; Rare:102 | ||||
| chr7:23014057-23014354 | Common:4; Rare:108; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:23105673-23105841 | Common:3; Rare:89; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181869-23182093 | Common:1; Rare:95 | ||||
| chr7:23470362-23470539 | Rare:55 | ||||
| chr7:23531958-23532083 | Common:1; Rare:50 | ||||
| chr7:24757397-24757636 | Common:2; Rare:70 | ||||
| chr7:24980108-24980414 | Common:8; Rare:129 | ||||
| chr7:25125209-25125649 | Rare:180; Clinvar:3 | ||||
| chr7:26200573-26200941 | Common:1; Rare:180 |