| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218381942-218382233 | Common:1; Rare:52 | ||||
| chr2:218568290-218568655 | Common:3; Rare:97 | ||||
| chr2:218568790-218568939 | Common:1; Rare:45 | ||||
| chr2:218659339-218659468 | Common:2; Rare:29 | ||||
| chr2:218659597-218659750 | Rare:37 | ||||
| chr2:218671973-218672334 | Common:2; Rare:90 | ||||
| chr2:219176899-219177118 | Common:4; Rare:67 | ||||
| chr2:219206683-219206916 | Rare:86 | ||||
| chr2:219229553-219229900 | Common:2; Rare:110 | ||||
| chr2:219245401-219245531 | Rare:36 | ||||
| chr2:219418682-219419018 | Common:2; Rare:109; Clinvar:19; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr2:219419863-219420162 | Common:2; Rare:63; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr2:219425636-219426019 | Common:2; Rare:80; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:219460609-219460858 | Common:3; Rare:58 | ||||
| chr2:219498691-219498919 | Common:2; Rare:46 |