| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107744035-107744198 | Rare:94 | ||||
| chr7:107891052-107891228 | Rare:149; Clinvar (benign):2 | ||||
| chr7:108003118-108003280 | Rare:85 | ||||
| chr7:108526032-108526416 | Common:10; Rare:233 | ||||
| chr7:108569547-108569999 | Common:5; Rare:323 | ||||
| chr7:111562432-111562617 | Common:4; Rare:160 | ||||
| chr7:112206255-112206727 | Common:4; Rare:255 | ||||
| chr7:112450285-112450477 | Common:8; Rare:123 | ||||
| chr7:112450775-112451080 | Common:4; Rare:155 | ||||
| chr7:112451100-112451610 | Common:9; Rare:208 | ||||
| chr7:112789870-112790160 | Common:2; Rare:155 | ||||
| chr7:112939680-112940180 | Common:7; Rare:265 | ||||
| chr7:114085713-114085909 | Common:2; Rare:80 | ||||
| chr7:114086000-114086549 | Common:3; Rare:261 | ||||
| chr7:114922399-114922646 | Common:1; Rare:82 |