| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:157257531-157257740 | Rare:37 | ||||
| chr2:158968476-158968702 | Rare:72 | ||||
| chr2:159286690-159286900 | Common:5; Rare:84 | ||||
| chr2:159615225-159615343 | Common:2; Rare:28 | ||||
| chr2:159615556-159615730 | Common:1; Rare:53 | ||||
| chr2:159616434-159616612 | Common:2; Rare:35 | ||||
| chr2:159712390-159712584 | Common:2; Rare:80 | ||||
| chr2:159798136-159798338 | Common:4; Rare:84 | ||||
| chr2:160493788-160493940 | Common:1; Rare:37 | ||||
| chr2:161308334-161308547 | Common:2; Rare:53 | ||||
| chr2:162073986-162074014 | Rare:11 | ||||
| chr2:163735995-163736048 | Rare:11 | ||||
| chr2:166375895-166376104 | Common:4; Rare:63; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:166494125-166494390 | Common:1; Rare:47 | ||||
| chr2:169584729-169584809 | Rare:20 |