| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201115900-201116454 | Common:2; Rare:101 | ||||
| chr2:201118607-201118825 | Rare:34 | ||||
| chr2:201258139-201258348 | Common:2; Rare:59; Clinvar (benign):2 | ||||
| chr2:201272491-201272682 | Rare:33; Clinvar:2 | ||||
| chr2:201451368-201451427 | Rare:17 | ||||
| chr2:201451435-201451907 | Common:3; Rare:113 | ||||
| chr2:201642653-201642734 | Rare:44 | ||||
| chr2:201780896-201780979 | Common:2; Rare:24; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:202238443-202238698 | Common:1; Rare:88; Clinvar:1 | ||||
| chr2:202265620-202265808 | Rare:70 | ||||
| chr2:202634733-202635021 | Common:6; Rare:103 | ||||
| chr2:202912147-202912304 | Common:1; Rare:54 | ||||
| chr2:202912438-202912558 | Common:2; Rare:38 | ||||
| chr2:203014676-203014944 | Common:1; Rare:81 | ||||
| chr2:203015348-203015535 | Rare:41 |