| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16465819-16465957 | Rare:21 | ||||
| chr7:16645658-16645971 | Rare:104 | ||||
| chr7:16881955-16882121 | Rare:42 | ||||
| chr7:17298444-17298738 | Common:3; Rare:79 | ||||
| chr7:17940395-17940584 | Common:1; Rare:93 | ||||
| chr7:20217343-20217597 | Common:1; Rare:55 | ||||
| chr7:20330657-20330737 | Rare:22 | ||||
| chr7:20331684-20331970 | Common:2; Rare:103 | ||||
| chr7:23105636-23105882 | Common:4; Rare:126; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181891-23182117 | Rare:92 | ||||
| chr7:23299193-23299409 | Common:2; Rare:114 | ||||
| chr7:23531925-23532083 | Common:2; Rare:67 | ||||
| chr7:24757417-24757552 | Common:1; Rare:44 | ||||
| chr7:24980108-24980360 | Common:6; Rare:104 | ||||
| chr7:25125235-25125633 | Rare:160; Clinvar:3 |