| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:171434550-171434677 | Rare:40; Clinvar:1 | ||||
| chr2:171434749-171434846 | Common:1; Rare:22 | ||||
| chr2:171522065-171522356 | Common:2; Rare:78 | ||||
| chr2:171894212-171894342 | Rare:58; Clinvar:1 | ||||
| chr2:171999806-171999980 | Common:1; Rare:72 | ||||
| chr2:172427304-172427731 | Common:10; Rare:113; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172427818-172427964 | Common:1; Rare:45 | ||||
| chr2:172556220-172556254 | Rare:8 | ||||
| chr2:172556682-172556820 | Rare:30 | ||||
| chr2:173964054-173964363 | Rare:136 | ||||
| chr2:173965244-173965539 | Common:2; Rare:106 | ||||
| chr2:174248454-174248747 | Common:1; Rare:88 | ||||
| chr2:174395618-174395887 | Common:2; Rare:86 | ||||
| chr2:174486987-174487409 | Common:2; Rare:104 | ||||
| chr2:174597710-174597960 | Rare:31 |