| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:43869464-43869663 | Rare:65 | ||||
| chr7:43926398-43926467 | Rare:24 | ||||
| chr7:44044554-44044754 | Common:3; Rare:66 | ||||
| chr7:44490608-44490700 | Rare:32 | ||||
| chr7:44573864-44574062 | Common:3; Rare:62 | ||||
| chr7:44582176-44582463 | Common:1; Rare:104 | ||||
| chr7:44606459-44606631 | Common:1; Rare:59 | ||||
| chr7:44748318-44748591 | Common:2; Rare:66 | ||||
| chr7:44796355-44796784 | Common:3; Rare:163 | ||||
| chr7:45000009-45000261 | Common:1; Rare:63 | ||||
| chr7:45111672-45111799 | Common:1; Rare:48 | ||||
| chr7:47582060-47582213 | Common:1; Rare:53 | ||||
| chr7:50450306-50450447 | Common:1; Rare:57 | ||||
| chr7:56051405-56051849 | Common:1; Rare:168; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56106414-56106680 | Common:7; Rare:94 |