| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218659326-218659363 | Rare:12 | ||||
| chr2:218659469-218659738 | Common:2; Rare:63 | ||||
| chr2:218671972-218672339 | Common:2; Rare:91 | ||||
| chr2:219176888-219177068 | Common:4; Rare:53 | ||||
| chr2:219178142-219178424 | Common:6; Rare:120 | ||||
| chr2:219206675-219206923 | Rare:90 | ||||
| chr2:219229577-219229905 | Common:2; Rare:101 | ||||
| chr2:219232183-219232293 | Common:1; Rare:40 | ||||
| chr2:219245413-219245511 | Rare:24 | ||||
| chr2:219253877-219254157 | Common:2; Rare:77 | ||||
| chr2:219419887-219420155 | Common:2; Rare:61; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:219420615-219420909 | Rare:77; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr2:219441890-219442080 | Rare:41 | ||||
| chr2:219443595-219443872 | Common:2; Rare:43 | ||||
| chr2:219445563-219445883 | Rare:56 |