| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169798767-169798965 | Rare:51 | ||||
| chr2:171433901-171434253 | Common:3; Rare:93 | ||||
| chr2:171434710-171434794 | Rare:25 | ||||
| chr2:171522324-171522520 | Common:2; Rare:41 | ||||
| chr2:171687702-171687930 | Rare:71 | ||||
| chr2:171894212-171894330 | Rare:56; Clinvar:1 | ||||
| chr2:171922279-171922503 | Rare:84 | ||||
| chr2:171999824-171999996 | Common:1; Rare:71 | ||||
| chr2:172084623-172084766 | Rare:36 | ||||
| chr2:172427420-172427849 | Common:7; Rare:129; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:173354584-173354912 | Common:1; Rare:97 | ||||
| chr2:173965350-173965531 | Common:1; Rare:77 | ||||
| chr2:174248460-174248769 | Common:1; Rare:97 | ||||
| chr2:174395629-174395808 | Common:1; Rare:58 | ||||
| chr2:174487022-174487438 | Common:2; Rare:109 |