| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107891064-107891235 | Rare:152; Clinvar (benign):4 | ||||
| chr7:108001250-108001890 | Common:4; Rare:201; Clinvar:1 | ||||
| chr7:108001941-108002761 | Common:6; Rare:269 | ||||
| chr7:108002861-108003341 | Common:6; Rare:279; Clinvar (benign):2 | ||||
| chr7:108003373-108003544 | Common:4; Rare:49 | ||||
| chr7:108003466-108003653 | Common:3; Rare:48 | ||||
| chr7:108456253-108456603 | Common:1; Rare:125 | ||||
| chr7:108526032-108526480 | Common:7; Rare:228 | ||||
| chr7:108569572-108570041 | Common:5; Rare:314 | ||||
| chr7:111562406-111562617 | Common:5; Rare:183 | ||||
| chr7:112206247-112206793 | Common:6; Rare:342 | ||||
| chr7:112422910-112423181 | Common:1; Rare:78 | ||||
| chr7:112450180-112450474 | Common:10; Rare:150 | ||||
| chr7:112450760-112451070 | Common:4; Rare:170 | ||||
| chr7:112789843-112790243 | Common:3; Rare:174 |