| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:116526202-116526403 | Common:2; Rare:54 | ||||
| chr7:117478928-117479161 | Common:1; Rare:43 | ||||
| chr7:117479297-117480112 | Common:3; Rare:178; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
| chr7:117872175-117872343 | Common:1; Rare:27 | ||||
| chr7:118183957-118184257 | Common:2; Rare:111 | ||||
| chr7:120857923-120858084 | Common:3; Rare:40; Clinvar:4 | ||||
| chr7:120858087-120858150 | Rare:12 | ||||
| chr7:120950491-120950833 | Common:3; Rare:107 | ||||
| chr7:120988664-120988931 | Common:1; Rare:56 | ||||
| chr7:121396262-121396514 | Common:1; Rare:81 | ||||
| chr7:122144207-122144433 | Common:1; Rare:48 | ||||
| chr7:123534552-123534833 | Common:5; Rare:60 | ||||
| chr7:123557773-123557994 | Common:1; Rare:54 | ||||
| chr7:123748600-123748824 | Common:1; Rare:80 | ||||
| chr7:123748833-123749298 | Common:3; Rare:161 |