| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:100023867-100024183 | Common:1; Rare:71 | ||||
| chr7:100049715-100049823 | Rare:43 | ||||
| chr7:100100518-100100852 | Common:1; Rare:140 | ||||
| chr7:100101320-100101720 | Common:1; Rare:157; Clinvar (benign):1 | ||||
| chr7:100119288-100119742 | Rare:141; Clinvar:1 | ||||
| chr7:100148716-100149064 | Common:1; Rare:151 | ||||
| chr7:100352335-100352619 | Common:4; Rare:54 | ||||
| chr7:100428264-100428514 | Common:2; Rare:66 | ||||
| chr7:100428636-100428944 | Common:4; Rare:122 | ||||
| chr7:100435961-100436274 | Common:1; Rare:109 | ||||
| chr7:100436485-100436819 | Rare:94 | ||||
| chr7:100585973-100586014 | Rare:12 | ||||
| chr7:100586096-100586304 | Common:1; Rare:75 | ||||
| chr7:100602311-100602401 | Common:1; Rare:24 | ||||
| chr7:100684448-100684774 | Rare:104 |