| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106112204-106112443 | Common:3; Rare:71 | ||||
| chr7:106112477-106112490 | Rare:7 | ||||
| chr7:106284885-106285529 | Common:6; Rare:233 | ||||
| chr7:106285537-106285542 | |||||
| chr7:107044515-107044985 | Common:2; Rare:171 | ||||
| chr7:107563846-107564047 | Common:2; Rare:118; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:107580126-107580316 | Common:2; Rare:69 | ||||
| chr7:107744053-107744180 | Rare:41 | ||||
| chr7:108526099-108526475 | Common:5; Rare:116 | ||||
| chr7:108569537-108570097 | Common:4; Rare:193 | ||||
| chr7:112206384-112206766 | Common:1; Rare:135 | ||||
| chr7:112450145-112450472 | Common:6; Rare:89 | ||||
| chr7:112939269-112939459 | Common:2; Rare:43 | ||||
| chr7:112939650-112940133 | Common:4; Rare:160 | ||||
| chr7:113918824-113919214 | Common:2; Rare:101; Clinvar (benign):1 |