| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:20330611-20330725 | Rare:25 | ||||
| chr7:20330771-20331061 | Common:2; Rare:81 | ||||
| chr7:20331731-20331870 | Common:1; Rare:51 | ||||
| chr7:22220180-22220365 | Common:2; Rare:31 | ||||
| chr7:23105667-23105871 | Common:4; Rare:108; Clinvar:2; Clinvar (benign):3 | ||||
| chr7:23106589-23106666 | Rare:13 | ||||
| chr7:23181805-23181869 | Common:1; Rare:18 | ||||
| chr7:23181921-23182128 | Rare:90 | ||||
| chr7:23299193-23299524 | Common:2; Rare:164 | ||||
| chr7:23470321-23470517 | Rare:62 | ||||
| chr7:23531948-23532083 | Common:1; Rare:54 | ||||
| chr7:23597219-23597510 | Common:1; Rare:94 | ||||
| chr7:24284163-24284239 | Rare:21 | ||||
| chr7:24757409-24757504 | Common:1; Rare:26 | ||||
| chr7:25125200-25125643 | Rare:180; Clinvar:3 |