| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:200889099-200889471 | Common:3; Rare:118 | ||||
| chr2:200963157-200963291 | Rare:12 | ||||
| chr2:200963509-200963785 | Common:1; Rare:76 | ||||
| chr2:201071548-201072047 | Rare:114 | ||||
| chr2:201116132-201116467 | Rare:62 | ||||
| chr2:201117099-201117184 | Rare:17 | ||||
| chr2:201118620-201118850 | Rare:32 | ||||
| chr2:201260429-201260585 | Rare:32 | ||||
| chr2:201451444-201451926 | Common:3; Rare:116 | ||||
| chr2:201642668-201642722 | Rare:28 | ||||
| chr2:202238504-202238670 | Rare:57 | ||||
| chr2:202265611-202265799 | Rare:64 | ||||
| chr2:202377078-202377357 | Common:2; Rare:59; Clinvar (benign):3 | ||||
| chr2:202634820-202635021 | Common:5; Rare:75 | ||||
| chr2:202912147-202912293 | Common:1; Rare:52 |