| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:112206339-112206762 | Common:2; Rare:141 | ||||
| chr7:112450338-112450537 | Common:1; Rare:75 | ||||
| chr7:112939705-112940112 | Common:4; Rare:136 | ||||
| chr7:116210330-116210640 | Common:4; Rare:84 | ||||
| chr7:116499434-116499857 | Common:3; Rare:144 | ||||
| chr7:116499898-116500326 | Common:3; Rare:110 | ||||
| chr7:116524495-116525105 | Rare:160 | ||||
| chr7:116525625-116526017 | Common:3; Rare:92 | ||||
| chr7:116526202-116526689 | Common:3; Rare:134; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr7:116672260-116672491 | Common:1; Rare:56; Clinvar:2 | ||||
| chr7:118183989-118184251 | Common:1; Rare:98 | ||||
| chr7:120857913-120858117 | Common:3; Rare:52; Clinvar:4 | ||||
| chr7:120951002-120951191 | Common:1; Rare:79 | ||||
| chr7:120988645-120989138 | Common:1; Rare:99 | ||||
| chr7:122144178-122144444 | Common:1; Rare:56 |