| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:103344328-103344503 | Rare:32 | ||||
| chr7:104207967-104208080 | Common:1; Rare:53 | ||||
| chr7:105013574-105013719 | Common:1; Rare:46 | ||||
| chr7:105014081-105014291 | Common:2; Rare:79 | ||||
| chr7:105532086-105532289 | Common:1; Rare:56 | ||||
| chr7:105876470-105876829 | Common:6; Rare:105 | ||||
| chr7:106112143-106112444 | Common:3; Rare:89 | ||||
| chr7:106112477-106112638 | Common:1; Rare:67 | ||||
| chr7:106284871-106285266 | Common:2; Rare:160 | ||||
| chr7:106285539-106285592 | Rare:14 | ||||
| chr7:107069653-107069862 | Common:2; Rare:31 | ||||
| chr7:107563861-107564028 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107580123-107580333 | Common:2; Rare:75 | ||||
| chr7:107743582-107743801 | Common:3; Rare:83 | ||||
| chr7:107744042-107744176 | Rare:46 |