| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:24757945-24758185 | Common:4; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:24980096-24980414 | Common:8; Rare:132 | ||||
| chr7:25125230-25125633 | Rare:164; Clinvar:3 | ||||
| chr7:26200694-26200941 | Rare:130 | ||||
| chr7:26201024-26201271 | Common:1; Rare:103 | ||||
| chr7:26201330-26201561 | Rare:84 | ||||
| chr7:26201590-26201818 | Common:2; Rare:118 | ||||
| chr7:26202083-26202402 | Rare:145 | ||||
| chr7:26864546-26864871 | Common:3; Rare:104 | ||||
| chr7:27096021-27096268 | Rare:63 | ||||
| chr7:27165435-27165685 | Common:4; Rare:94 | ||||
| chr7:27740037-27740199 | Common:5; Rare:47 | ||||
| chr7:29989732-29989898 | Rare:66 | ||||
| chr7:30478681-30478811 | Common:1; Rare:47 | ||||
| chr7:30504758-30505081 | Common:2; Rare:106 |