| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106284969-106285455 | Common:6; Rare:167 | ||||
| chr7:107563889-107564022 | Common:2; Rare:78; Clinvar (benign):3 | ||||
| chr7:107744058-107744164 | Rare:36 | ||||
| chr7:108569615-108569931 | Common:1; Rare:101 | ||||
| chr7:112206389-112206713 | Common:1; Rare:106 | ||||
| chr7:112450241-112450470 | Common:4; Rare:71 | ||||
| chr7:116210405-116210591 | Common:3; Rare:47 | ||||
| chr7:116499509-116499779 | Common:3; Rare:92 | ||||
| chr7:116526202-116526405 | Common:2; Rare:54 | ||||
| chr7:116672274-116672514 | Common:1; Rare:60; Clinvar:2 | ||||
| chr7:118183965-118184179 | Common:1; Rare:79 | ||||
| chr7:121396271-121396498 | Common:1; Rare:70 | ||||
| chr7:123557773-123558016 | Common:1; Rare:61 | ||||
| chr7:123748987-123749214 | Common:2; Rare:79 | ||||
| chr7:127651972-127652208 | Rare:72 |