| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:122886462-122886603 | Rare:39 | ||||
| chr7:123534332-123534370 | Rare:7 | ||||
| chr7:123534537-123534833 | Common:5; Rare:63 | ||||
| chr7:123557741-123558106 | Common:2; Rare:90 | ||||
| chr7:123748723-123748822 | Rare:36 | ||||
| chr7:123748841-123749285 | Common:3; Rare:154 | ||||
| chr7:124929793-124929921 | Common:3; Rare:45 | ||||
| chr7:124929931-124929985 | Rare:14 | ||||
| chr7:127585575-127585707 | Common:2; Rare:44 | ||||
| chr7:127588283-127588502 | Rare:94 | ||||
| chr7:127588994-127589132 | Rare:43 | ||||
| chr7:127651842-127652227 | Common:3; Rare:111 | ||||
| chr7:128409819-128410076 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:128455663-128455903 | Common:3; Rare:116 | ||||
| chr7:128739152-128739432 | Common:2; Rare:73 |