| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:101210619-101210733 | Common:1; Rare:34; Clinvar (benign):1 | ||||
| chr7:101217847-101218201 | Common:4; Rare:114 | ||||
| chr7:101244984-101245168 | Common:1; Rare:80 | ||||
| chr7:101252254-101252432 | Rare:41 | ||||
| chr7:101321733-101321848 | Common:2; Rare:41 | ||||
| chr7:101815583-101816090 | Common:3; Rare:141 | ||||
| chr7:102464837-102465014 | Common:1; Rare:72 | ||||
| chr7:102748675-102749051 | Common:3; Rare:90 | ||||
| chr7:102749063-102749331 | Common:3; Rare:75 | ||||
| chr7:103074794-103074884 | Rare:37 | ||||
| chr7:103148976-103149386 | Common:5; Rare:123 | ||||
| chr7:103149464-103149758 | Common:2; Rare:76 | ||||
| chr7:103319616-103319874 | Rare:65 | ||||
| chr7:103344709-103344869 | Common:1; Rare:52 | ||||
| chr7:104207959-104208116 | Common:3; Rare:71 |