| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200888986-200889455 | Common:3; Rare:147 | ||||
| chr2:200963536-200963905 | Common:1; Rare:101 | ||||
| chr2:201071615-201072047 | Rare:91 | ||||
| chr2:201118576-201118825 | Rare:43 | ||||
| chr2:201451444-201451920 | Common:3; Rare:116 | ||||
| chr2:201642637-201642732 | Rare:49 | ||||
| chr2:201780887-201781243 | Common:3; Rare:109; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:202238443-202238621 | Rare:61; Clinvar:1 | ||||
| chr2:202265462-202265790 | Common:1; Rare:91 | ||||
| chr2:202911613-202911740 | Rare:20 | ||||
| chr2:202911886-202912291 | Common:2; Rare:111 | ||||
| chr2:202912510-202912548 | Rare:12 | ||||
| chr2:203238779-203239042 | Common:1; Rare:93 | ||||
| chr2:203239213-203239344 | Rare:42 | ||||
| chr2:203328063-203328531 | Common:2; Rare:163 |