| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218399557-218399657 | Common:1; Rare:41 | ||||
| chr2:218568290-218568972 | Common:5; Rare:179 | ||||
| chr2:218659339-218659363 | Rare:8 | ||||
| chr2:218659530-218659737 | Common:1; Rare:48 | ||||
| chr2:218671966-218672327 | Common:2; Rare:91 | ||||
| chr2:219176845-219177110 | Common:4; Rare:80 | ||||
| chr2:219178142-219178461 | Common:6; Rare:133 | ||||
| chr2:219224008-219224191 | Rare:56 | ||||
| chr2:219229330-219229397 | Rare:21 | ||||
| chr2:219229535-219229900 | Common:2; Rare:116 | ||||
| chr2:219245442-219245516 | Rare:22 | ||||
| chr2:219253859-219254056 | Common:1; Rare:62 | ||||
| chr2:219418347-219419040 | Common:5; Rare:230; Clinvar:40; Clinvar (benign):22; Clinvar (pathogenic):3 | ||||
| chr2:219419713-219419788 | Common:1; Rare:8 | ||||
| chr2:219419854-219420183 | Common:2; Rare:70; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):2 |