| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:16645658-16646229 | Common:5; Rare:201 | ||||
| chr7:17940435-17940574 | Common:1; Rare:68 | ||||
| chr7:20217347-20217577 | Common:1; Rare:51 | ||||
| chr7:20331754-20331846 | Common:1; Rare:34 | ||||
| chr7:23105682-23105875 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23181711-23182096 | Common:2; Rare:134 | ||||
| chr7:23470362-23470539 | Rare:55 | ||||
| chr7:23531948-23532083 | Common:1; Rare:54 | ||||
| chr7:23597310-23597412 | Rare:34 | ||||
| chr7:24283959-24284264 | Rare:86 | ||||
| chr7:25125235-25125620 | Rare:154; Clinvar:3 | ||||
| chr7:26200628-26200939 | Common:1; Rare:151 | ||||
| chr7:26201187-26201555 | Rare:145 | ||||
| chr7:26201570-26201805 | Common:2; Rare:126 | ||||
| chr7:26291835-26292025 | Common:2; Rare:67 |