| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:166494038-166494380 | Common:1; Rare:59 | ||||
| chr2:167187221-167187496 | Common:2; Rare:50 | ||||
| chr2:169584303-169584630 | Common:1; Rare:124 | ||||
| chr2:169584696-169584816 | Rare:31 | ||||
| chr2:169694360-169694597 | Common:5; Rare:76 | ||||
| chr2:170928899-170929349 | Common:5; Rare:128 | ||||
| chr2:171160356-171160646 | Common:1; Rare:92 | ||||
| chr2:171433967-171434352 | Common:2; Rare:102 | ||||
| chr2:171434736-171434861 | Common:1; Rare:27 | ||||
| chr2:171522272-171522547 | Common:3; Rare:67 | ||||
| chr2:171894201-171894341 | Rare:65; Clinvar:2 | ||||
| chr2:171922288-171922506 | Rare:82 | ||||
| chr2:171999831-171999985 | Common:1; Rare:63 | ||||
| chr2:172427233-172427725 | Common:10; Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:172735674-172735985 | Common:2; Rare:82 |