| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:202912125-202912571 | Common:4; Rare:133 | ||||
| chr2:203014626-203014915 | Common:1; Rare:87 | ||||
| chr2:203239212-203239312 | Rare:31 | ||||
| chr2:203328138-203328434 | Common:2; Rare:111 | ||||
| chr2:203535208-203535546 | Common:3; Rare:138 | ||||
| chr2:206085938-206085965 | Rare:4 | ||||
| chr2:206159386-206159982 | Common:3; Rare:180 | ||||
| chr2:206765273-206765645 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:207165943-207166138 | Rare:37 | ||||
| chr2:207529808-207530104 | Common:1; Rare:82 | ||||
| chr2:208254944-208255238 | Common:2; Rare:73 | ||||
| chr2:208266036-208266313 | Common:9; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209771728-209772009 | Common:1; Rare:80 | ||||
| chr2:210225333-210225403 | Rare:12 | ||||
| chr2:210225405-210225746 | Rare:58 |