| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:112939776-112940176 | Common:3; Rare:111 | ||||
| chr7:114922011-114922199 | Rare:45 | ||||
| chr7:116952682-116953024 | Rare:52 | ||||
| chr7:116953044-116953350 | Common:2; Rare:46 | ||||
| chr7:116954283-116954303 | Rare:4 | ||||
| chr7:116954315-116954358 | Common:1; Rare:12 | ||||
| chr7:117479792-117480052 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:117872161-117872378 | Common:2; Rare:43 | ||||
| chr7:118183866-118184238 | Common:6; Rare:152 | ||||
| chr7:120273697-120273740 | Rare:13 | ||||
| chr7:120857903-120858182 | Common:3; Rare:69; Clinvar:4 | ||||
| chr7:120950488-120950838 | Common:3; Rare:109 | ||||
| chr7:121396281-121396498 | Common:1; Rare:66 | ||||
| chr7:121872712-121872982 | Common:3; Rare:47 | ||||
| chr7:121873200-121873289 | Common:2; Rare:19 |