| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169733713-169733932 | Common:2; Rare:71 | ||||
| chr2:169798788-169798965 | Rare:45 | ||||
| chr2:170929007-170929318 | Common:4; Rare:105 | ||||
| chr2:171433849-171434239 | Common:3; Rare:100 | ||||
| chr2:171434749-171434810 | Rare:14 | ||||
| chr2:171522197-171522473 | Common:3; Rare:70 | ||||
| chr2:171894217-171894376 | Rare:68; Clinvar:1 | ||||
| chr2:171922315-171922507 | Rare:72 | ||||
| chr2:171999837-171999972 | Common:1; Rare:55 | ||||
| chr2:172427457-172427711 | Common:4; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:173354562-173354908 | Common:1; Rare:104 | ||||
| chr2:173965345-173965531 | Common:1; Rare:79 | ||||
| chr2:174248454-174248779 | Common:1; Rare:105 | ||||
| chr2:174395629-174395800 | Common:1; Rare:57 | ||||
| chr2:175005156-175005294 | Rare:44; Clinvar:2 |