| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218659600-218659750 | Rare:36 | ||||
| chr2:218671972-218672339 | Common:2; Rare:91 | ||||
| chr2:219160778-219160869 | Common:1; Rare:32 | ||||
| chr2:219176918-219177109 | Common:4; Rare:59 | ||||
| chr2:219206670-219206923 | Rare:91 | ||||
| chr2:219229577-219229900 | Common:2; Rare:98 | ||||
| chr2:219245401-219245531 | Rare:36 | ||||
| chr2:219419918-219420140 | Common:1; Rare:50; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:219498670-219498925 | Common:2; Rare:53 | ||||
| chr2:219597719-219597904 | Common:1; Rare:74 | ||||
| chr2:222656049-222656446 | Common:3; Rare:127 | ||||
| chr2:223957257-223957475 | Common:4; Rare:81 | ||||
| chr2:226835911-226836117 | Common:1; Rare:82 | ||||
| chr2:227325191-227325340 | Common:4; Rare:52 | ||||
| chr2:227871577-227871684 | Common:5; Rare:40 |