| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105014065-105014292 | Common:2; Rare:87 | ||||
| chr7:105532055-105532269 | Common:3; Rare:58 | ||||
| chr7:105679081-105679209 | Common:1; Rare:37 | ||||
| chr7:105876470-105876844 | Common:6; Rare:109 | ||||
| chr7:105877371-105877503 | Common:2; Rare:19 | ||||
| chr7:106112477-106112650 | Common:1; Rare:70 | ||||
| chr7:106284122-106284255 | Rare:38 | ||||
| chr7:106284883-106285262 | Common:2; Rare:153 | ||||
| chr7:106285539-106285668 | Rare:30 | ||||
| chr7:107044946-107045213 | Common:3; Rare:87 | ||||
| chr7:107168775-107169027 | Rare:85 | ||||
| chr7:107563865-107564028 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107564313-107564347 | Rare:7; Clinvar:1 | ||||
| chr7:107580126-107580294 | Common:2; Rare:67 | ||||
| chr7:107743604-107743852 | Common:4; Rare:95 |