| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:8262505-8262672 | Common:2; Rare:45 | ||||
| chr7:10940059-10940589 | Common:5; Rare:207; Clinvar (benign):3 | ||||
| chr7:10973815-10973941 | Rare:51 | ||||
| chr7:11831812-11832070 | Common:3; Rare:79 | ||||
| chr7:12211160-12211425 | Common:3; Rare:113 | ||||
| chr7:12403874-12403960 | Common:1; Rare:19 | ||||
| chr7:12610979-12611125 | Rare:30 | ||||
| chr7:12686733-12687043 | Common:3; Rare:98 | ||||
| chr7:12687081-12687325 | Common:2; Rare:59 | ||||
| chr7:12687470-12687619 | Common:3; Rare:39 | ||||
| chr7:13991327-13991642 | Common:3; Rare:88 | ||||
| chr7:15396569-15396812 | Common:2; Rare:101 | ||||
| chr7:16526719-16526883 | Common:2; Rare:37 | ||||
| chr7:16645696-16646220 | Common:4; Rare:187 | ||||
| chr7:16646518-16646589 | Common:1; Rare:18 |