| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101085341-101085521 | Common:1; Rare:34 | ||||
| chr7:101164766-101165737 | Common:3; Rare:224 | ||||
| chr7:101210092-101210369 | Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:101216479-101216730 | Rare:95 | ||||
| chr7:101217306-101217564 | Common:1; Rare:65 | ||||
| chr7:101217847-101218216 | Common:4; Rare:120 | ||||
| chr7:101244984-101245191 | Common:1; Rare:86 | ||||
| chr7:101252266-101252516 | Common:1; Rare:55 | ||||
| chr7:101321705-101321848 | Common:2; Rare:51 | ||||
| chr7:101815567-101816090 | Common:3; Rare:148 | ||||
| chr7:102464835-102465014 | Common:1; Rare:72 | ||||
| chr7:102572547-102572810 | Common:3; Rare:21 | ||||
| chr7:102748663-102749035 | Common:3; Rare:85 | ||||
| chr7:103074517-103074882 | Rare:109 | ||||
| chr7:103148998-103149386 | Common:5; Rare:118 |