| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:123534573-123534829 | Common:5; Rare:52 | ||||
| chr7:123748723-123748746 | Rare:9 | ||||
| chr7:123748757-123748829 | Rare:22 | ||||
| chr7:123748873-123749278 | Common:3; Rare:145 | ||||
| chr7:124929792-124929911 | Common:2; Rare:39 | ||||
| chr7:124929913-124929990 | Rare:21 | ||||
| chr7:127392071-127392346 | Rare:110 | ||||
| chr7:127585546-127585689 | Common:2; Rare:56 | ||||
| chr7:127588254-127588490 | Rare:98 | ||||
| chr7:127651806-127652231 | Common:3; Rare:128 | ||||
| chr7:128405913-128406105 | Common:2; Rare:70 | ||||
| chr7:128409915-128410142 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455653-128455965 | Common:3; Rare:150 | ||||
| chr7:128476645-128476871 | Common:1; Rare:88 | ||||
| chr7:128739146-128739427 | Common:2; Rare:75 |