| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:19709017-19709171 | Common:4; Rare:53 | ||||
| chr7:20330369-20331065 | Common:4; Rare:176 | ||||
| chr7:20331692-20331856 | Common:2; Rare:53 | ||||
| chr7:20786881-20787072 | Common:1; Rare:59 | ||||
| chr7:22822757-22822969 | Common:3; Rare:78 | ||||
| chr7:23105667-23105865 | Common:4; Rare:106; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23106589-23106670 | Rare:14 | ||||
| chr7:23181941-23182173 | Rare:100 | ||||
| chr7:23299197-23299361 | Common:2; Rare:79 | ||||
| chr7:23470302-23470586 | Common:1; Rare:88 | ||||
| chr7:23531954-23532092 | Common:1; Rare:55 | ||||
| chr7:23597307-23597505 | Common:1; Rare:69 | ||||
| chr7:24283525-24283763 | Common:4; Rare:48 | ||||
| chr7:24284010-24284024 | Rare:4 | ||||
| chr7:24284038-24284269 | Rare:70 |