| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:103324489-103324667 | Rare:40 | ||||
| chr7:105014097-105014304 | Common:1; Rare:76 | ||||
| chr7:105522192-105522326 | Common:1; Rare:51 | ||||
| chr7:105532078-105532250 | Common:1; Rare:44 | ||||
| chr7:105876470-105876829 | Common:6; Rare:105 | ||||
| chr7:106284844-106285250 | Common:2; Rare:153 | ||||
| chr7:106285539-106285592 | Rare:14 | ||||
| chr7:106285639-106285899 | Common:2; Rare:46 | ||||
| chr7:106661141-106661324 | Common:1; Rare:32 | ||||
| chr7:107563840-107564028 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):5 | ||||
| chr7:107580147-107580294 | Common:2; Rare:59 | ||||
| chr7:107744018-107744176 | Rare:50 | ||||
| chr7:107929063-107929524 | Common:4; Rare:135; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:108526099-108526433 | Common:5; Rare:107 | ||||
| chr7:108569592-108570067 | Common:2; Rare:165 |