| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169824824-169825055 | Common:4; Rare:70 | ||||
| chr2:171433941-171434248 | Common:3; Rare:79 | ||||
| chr2:171687961-171688026 | Common:1; Rare:14 | ||||
| chr2:171894212-171894393 | Rare:78; Clinvar:1 | ||||
| chr2:171922283-171922503 | Rare:83 | ||||
| chr2:171999831-171999972 | Common:1; Rare:58 | ||||
| chr2:172427444-172427736 | Common:6; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172427773-172427839 | Rare:25; Clinvar:2 | ||||
| chr2:173354586-173354918 | Common:1; Rare:100 | ||||
| chr2:173965356-173965531 | Common:1; Rare:75 | ||||
| chr2:174248454-174248779 | Common:1; Rare:105 | ||||
| chr2:174395624-174395800 | Common:2; Rare:58 | ||||
| chr2:174410259-174410430 | Common:4; Rare:48 | ||||
| chr2:174487037-174487404 | Common:2; Rare:91 | ||||
| chr2:175181637-175181820 | Common:3; Rare:69 |