| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:24980119-24980441 | Common:8; Rare:128 | ||||
| chr7:25125206-25125561 | Rare:151; Clinvar:3 | ||||
| chr7:26200564-26201555 | Common:3; Rare:432 | ||||
| chr7:26201619-26201805 | Common:1; Rare:99 | ||||
| chr7:26864439-26864856 | Common:3; Rare:125 | ||||
| chr7:27096017-27096199 | Rare:57 | ||||
| chr7:27152556-27152741 | Rare:33 | ||||
| chr7:27179840-27179987 | Rare:55 | ||||
| chr7:27740037-27740209 | Common:5; Rare:49 | ||||
| chr7:28686027-28686177 | Rare:39 | ||||
| chr7:30478681-30478839 | Common:1; Rare:58 | ||||
| chr7:30504698-30505079 | Common:4; Rare:128 | ||||
| chr7:30594722-30595084 | Common:6; Rare:169; Clinvar:9; Clinvar (benign):13 | ||||
| chr7:30911629-30911890 | Common:1; Rare:59 | ||||
| chr7:32495240-32495587 | Rare:89 |