| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:120858203-120858246 | Rare:6 | ||||
| chr7:120858304-120858474 | Common:1; Rare:23 | ||||
| chr7:120950509-120950819 | Common:2; Rare:98 | ||||
| chr7:121396234-121396543 | Common:1; Rare:105 | ||||
| chr7:122144229-122144426 | Common:1; Rare:41 | ||||
| chr7:123557773-123558027 | Common:1; Rare:64 | ||||
| chr7:123748912-123749298 | Common:3; Rare:138 | ||||
| chr7:124929776-124929929 | Common:3; Rare:50 | ||||
| chr7:124929981-124930094 | Rare:26 | ||||
| chr7:127585584-127585694 | Rare:33 | ||||
| chr7:127588292-127588489 | Rare:84 | ||||
| chr7:127651823-127652235 | Common:3; Rare:122 | ||||
| chr7:128409920-128410241 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:128455729-128455931 | Common:2; Rare:113 | ||||
| chr7:128476656-128476777 | Rare:44 |