| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:102671631-102671869 | Common:8; Rare:34 | ||||
| chr7:102748692-102749020 | Common:2; Rare:70 | ||||
| chr7:103344672-103344865 | Common:1; Rare:67 | ||||
| chr7:104207952-104208077 | Common:2; Rare:62 | ||||
| chr7:105014091-105014236 | Common:1; Rare:61 | ||||
| chr7:105532070-105532238 | Rare:45 | ||||
| chr7:105876481-105876851 | Common:7; Rare:108 | ||||
| chr7:106112477-106112494 | Rare:9 | ||||
| chr7:106284525-106284767 | Common:3; Rare:70 | ||||
| chr7:106284978-106285234 | Common:2; Rare:90 | ||||
| chr7:106285539-106285561 | Rare:7 | ||||
| chr7:107563888-107564025 | Common:2; Rare:82; Clinvar (benign):4 | ||||
| chr7:107580147-107580287 | Common:2; Rare:55 | ||||
| chr7:107744018-107744176 | Rare:50 | ||||
| chr7:107891058-107891225 | Rare:81; Clinvar (benign):2 |