| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218568726-218568961 | Common:1; Rare:66 | ||||
| chr2:218659339-218659750 | Common:4; Rare:97 | ||||
| chr2:218671972-218672334 | Common:2; Rare:91 | ||||
| chr2:218782011-218782321 | Rare:95; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:219160772-219160935 | Common:1; Rare:48 | ||||
| chr2:219176855-219177127 | Common:4; Rare:82 | ||||
| chr2:219177819-219177929 | Common:3; Rare:22 | ||||
| chr2:219178090-219178464 | Common:7; Rare:152 | ||||
| chr2:219206683-219206923 | Rare:87 | ||||
| chr2:219229330-219229419 | Rare:29 | ||||
| chr2:219229559-219229900 | Common:2; Rare:107 | ||||
| chr2:219245383-219245531 | Rare:43 | ||||
| chr2:219253861-219254056 | Common:1; Rare:61 | ||||
| chr2:219278994-219279159 | Rare:35 | ||||
| chr2:219279240-219279595 | Common:3; Rare:118; Clinvar (benign):1 |