| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:23597228-23597412 | Rare:56 | ||||
| chr7:24980147-24980414 | Common:8; Rare:111 | ||||
| chr7:25125204-25125643 | Rare:180; Clinvar:3 | ||||
| chr7:26152713-26153008 | Rare:89 | ||||
| chr7:26200572-26201102 | Common:2; Rare:248 | ||||
| chr7:26201323-26201830 | Common:2; Rare:225 | ||||
| chr7:26202083-26202402 | Rare:145 | ||||
| chr7:27662737-27662812 | Common:1; Rare:20 | ||||
| chr7:27740037-27740216 | Common:5; Rare:56 | ||||
| chr7:29563654-29563848 | Common:1; Rare:51 | ||||
| chr7:30504754-30505079 | Common:2; Rare:108 | ||||
| chr7:30594718-30595134 | Common:6; Rare:186; Clinvar:11; Clinvar (benign):14 | ||||
| chr7:30771302-30771453 | Common:1; Rare:47 | ||||
| chr7:32495238-32495624 | Common:1; Rare:99 | ||||
| chr7:32495713-32496011 | Common:3; Rare:77 |