| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:159904706-159904848 | Rare:35 | ||||
| chr2:160062437-160062729 | Common:6; Rare:80 | ||||
| chr2:160493794-160493890 | Rare:21 | ||||
| chr2:161308325-161308508 | Common:2; Rare:47 | ||||
| chr2:162243403-162243577 | Common:1; Rare:27 | ||||
| chr2:162318729-162318804 | Rare:17 | ||||
| chr2:163735995-163736043 | Rare:9 | ||||
| chr2:164841192-164841382 | Rare:55 | ||||
| chr2:164841798-164841851 | Rare:8 | ||||
| chr2:165794128-165794342 | Common:2; Rare:58; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:165953748-165953841 | Rare:49; Clinvar:6 | ||||
| chr2:166494092-166494441 | Common:1; Rare:63 | ||||
| chr2:168456130-168456437 | Rare:107 | ||||
| chr2:169584564-169584646 | Rare:20 | ||||
| chr2:169584755-169584844 | Rare:28 |