| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:164840548-164840749 | Common:1; Rare:37 | ||||
| chr2:164841192-164841510 | Rare:92 | ||||
| chr2:164841801-164841960 | Common:1; Rare:44 | ||||
| chr2:165794091-165794376 | Common:2; Rare:79; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:165794729-165794787 | Rare:13 | ||||
| chr2:165795139-165795393 | Common:1; Rare:42 | ||||
| chr2:165953723-165953847 | Rare:62; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:168247540-168247792 | Common:4; Rare:90 | ||||
| chr2:168456125-168456437 | Rare:107 | ||||
| chr2:168456539-168456614 | Rare:23 | ||||
| chr2:168890428-168890462 | Rare:5 | ||||
| chr2:169066886-169067198 | Common:1; Rare:60 | ||||
| chr2:169584303-169584630 | Common:1; Rare:124 | ||||
| chr2:169584744-169584816 | Rare:18 | ||||
| chr2:169694340-169694597 | Common:5; Rare:87 |