| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:10940332-10940579 | Common:1; Rare:87 | ||||
| chr7:11831789-11832070 | Common:3; Rare:89 | ||||
| chr7:12211151-12211470 | Common:3; Rare:124 | ||||
| chr7:12403824-12404018 | Common:1; Rare:46 | ||||
| chr7:12686579-12687003 | Common:4; Rare:130 | ||||
| chr7:15686514-15686791 | Common:3; Rare:78 | ||||
| chr7:15686793-15686936 | Rare:41 | ||||
| chr7:16421212-16421558 | Common:2; Rare:87; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr7:16645628-16646223 | Common:4; Rare:204 | ||||
| chr7:17298444-17298730 | Common:3; Rare:76 | ||||
| chr7:17299129-17299195 | Rare:15 | ||||
| chr7:17940390-17940618 | Common:2; Rare:112 | ||||
| chr7:17940656-17940799 | Common:4; Rare:38 | ||||
| chr7:20217337-20217598 | Common:1; Rare:56 | ||||
| chr7:20330665-20331061 | Common:2; Rare:109 |