| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107776931-107777134 | Common:1; Rare:34 | ||||
| chr7:107803078-107803540 | Common:4; Rare:90 | ||||
| chr7:107929152-107929711 | Common:3; Rare:158; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:107937152-107937380 | Rare:62; Clinvar (benign):1 | ||||
| chr7:108003104-108003280 | Rare:55 | ||||
| chr7:108526039-108526486 | Common:5; Rare:133 | ||||
| chr7:108569576-108570006 | Common:2; Rare:156 | ||||
| chr7:111562463-111562664 | Rare:73 | ||||
| chr7:112206339-112206719 | Common:2; Rare:119 | ||||
| chr7:112450288-112450491 | Common:4; Rare:69 | ||||
| chr7:112790015-112790118 | Rare:32 | ||||
| chr7:112790322-112790560 | Common:1; Rare:71 | ||||
| chr7:112939712-112940109 | Common:4; Rare:133 | ||||
| chr7:114086040-114086545 | Common:2; Rare:158 | ||||
| chr7:116499514-116499779 | Common:3; Rare:90 |