| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101085328-101085590 | Common:3; Rare:75 | ||||
| chr7:101126200-101126800 | Common:9; Rare:243; Clinvar (pathogenic):2 | ||||
| chr7:101126974-101127110 | Common:2; Rare:50 | ||||
| chr7:101216184-101216457 | Common:1; Rare:100 | ||||
| chr7:101217849-101218216 | Common:8; Rare:232 | ||||
| chr7:101244969-101245225 | Common:2; Rare:179 | ||||
| chr7:101252264-101252540 | Common:2; Rare:110 | ||||
| chr7:101321710-101321890 | Common:6; Rare:126 | ||||
| chr7:101815561-101816040 | Common:6; Rare:271 | ||||
| chr7:101816210-101816730 | Common:10; Rare:185 | ||||
| chr7:101817330-101817688 | Common:1; Rare:140 | ||||
| chr7:102273860-102274280 | Common:6; Rare:152 | ||||
| chr7:102286000-102286420 | Rare:133 | ||||
| chr7:102286693-102286958 | Common:9; Rare:87 | ||||
| chr7:102363609-102363979 | Common:2; Rare:196 |