| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:172084190-172084470 | Common:3; Rare:100 | ||||
| chr2:172084562-172084877 | Rare:155 | ||||
| chr2:172085187-172085559 | Common:3; Rare:93 | ||||
| chr2:172102488-172102696 | Common:2; Rare:78 | ||||
| chr2:172102710-172103109 | Common:6; Rare:187 | ||||
| chr2:172427409-172427751 | Common:12; Rare:161; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:172427960-172428593 | Common:15; Rare:250; Clinvar (benign):2 | ||||
| chr2:172555767-172556185 | Common:8; Rare:356 | ||||
| chr2:172556423-172556880 | Common:2; Rare:197 | ||||
| chr2:172735365-172735614 | Common:3; Rare:42 | ||||
| chr2:172735750-172735935 | Common:1; Rare:45 | ||||
| chr2:172859340-172859860 | Common:3; Rare:77 | ||||
| chr2:172859880-172860270 | Common:1; Rare:66 | ||||
| chr2:172927822-172928447 | Common:10; Rare:213 | ||||
| chr2:173075185-173075627 | Common:13; Rare:159 |