| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105014070-105014261 | Common:2; Rare:79 | ||||
| chr7:105532070-105532260 | Common:1; Rare:50 | ||||
| chr7:105876477-105876819 | Common:6; Rare:101 | ||||
| chr7:106112204-106112644 | Common:4; Rare:158 | ||||
| chr7:106284531-106284840 | Common:4; Rare:92 | ||||
| chr7:106284890-106285276 | Common:2; Rare:155 | ||||
| chr7:106285539-106285545 | |||||
| chr7:106661150-106661273 | Common:1; Rare:17 | ||||
| chr7:107563888-107564028 | Common:2; Rare:83; Clinvar (benign):4 | ||||
| chr7:107580147-107580316 | Common:2; Rare:61 | ||||
| chr7:107743588-107743801 | Common:3; Rare:80 | ||||
| chr7:107744053-107744176 | Rare:41 | ||||
| chr7:107891389-107891430 | Rare:13 | ||||
| chr7:108526099-108526475 | Common:5; Rare:116 | ||||
| chr7:108569576-108570013 | Common:2; Rare:157 |