| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169694367-169694606 | Common:5; Rare:75 | ||||
| chr2:170928899-170929331 | Common:5; Rare:125 | ||||
| chr2:171433951-171434328 | Common:2; Rare:99 | ||||
| chr2:171434724-171434839 | Common:1; Rare:27 | ||||
| chr2:171522369-171522630 | Common:2; Rare:74 | ||||
| chr2:171687989-171688064 | Rare:20 | ||||
| chr2:171894210-171894407 | Rare:88; Clinvar:1 | ||||
| chr2:171999833-171999985 | Common:1; Rare:62 | ||||
| chr2:172427415-172427725 | Common:7; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:173075212-173075561 | Common:5; Rare:64 | ||||
| chr2:173964092-173964309 | Rare:99 | ||||
| chr2:173965266-173965370 | Rare:29 | ||||
| chr2:174395629-174395800 | Common:1; Rare:57 | ||||
| chr2:174486987-174487380 | Common:2; Rare:92 | ||||
| chr2:175005135-175005331 | Rare:68; Clinvar:2 |