| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107563861-107564028 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107580144-107580331 | Common:2; Rare:69 | ||||
| chr7:107744042-107744171 | Rare:42 | ||||
| chr7:108526099-108526416 | Common:5; Rare:104 | ||||
| chr7:108569576-108569999 | Common:2; Rare:154 | ||||
| chr7:112206384-112206789 | Common:1; Rare:147 | ||||
| chr7:112450291-112450460 | Common:4; Rare:56 | ||||
| chr7:116499514-116499796 | Common:3; Rare:95 | ||||
| chr7:116499869-116500139 | Common:2; Rare:70 | ||||
| chr7:116524495-116525092 | Rare:155 | ||||
| chr7:116525218-116525510 | Common:2; Rare:83 | ||||
| chr7:116525602-116525739 | Rare:29 | ||||
| chr7:116672274-116672443 | Common:1; Rare:43; Clinvar:2 | ||||
| chr7:116953423-116953517 | Rare:36 | ||||
| chr7:118183965-118184217 | Common:2; Rare:100 |