| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:17374535-17374764 | Common:2; Rare:50 | ||||
| chr7:17414846-17414876 | Rare:5 | ||||
| chr7:17419019-17419059 | Rare:10 | ||||
| chr7:17436279-17436326 | Rare:11 | ||||
| chr7:17439980-17439983 | |||||
| chr7:20002810-20003057 | Common:1; Rare:40 | ||||
| chr7:22174617-22174696 | Rare:10 | ||||
| chr7:23490286-23490570 | Common:3; Rare:90 | ||||
| chr7:23680810-23680976 | Common:2; Rare:40 | ||||
| chr7:24820196-24820487 | Common:3; Rare:68 | ||||
| chr7:24979500-24979557 | Common:1; Rare:20 | ||||
| chr7:26188711-26188736 | Rare:2 | ||||
| chr7:26193226-26193701 | Rare:166; Clinvar (benign):2 | ||||
| chr7:26199922-26199940 | Rare:6 | ||||
| chr7:28956512-28956790 | Common:3; Rare:104 |