| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218568713-218568969 | Common:1; Rare:70 | ||||
| chr2:218569058-218569393 | Common:4; Rare:97 | ||||
| chr2:218658943-218658975 | Rare:2 | ||||
| chr2:218659359-218659411 | Common:1; Rare:10 | ||||
| chr2:218659418-218659845 | Common:2; Rare:108 | ||||
| chr2:218671712-218671746 | Rare:10 | ||||
| chr2:218671928-218672349 | Common:2; Rare:121 | ||||
| chr2:218710687-218711085 | Common:4; Rare:93 | ||||
| chr2:218711244-218711368 | Common:1; Rare:26 | ||||
| chr2:218781981-218782183 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:218880054-218880370 | Common:2; Rare:47 | ||||
| chr2:218880467-218880643 | Common:4; Rare:46; Clinvar (benign):1 | ||||
| chr2:218883566-218883678 | Common:1; Rare:39 | ||||
| chr2:218892761-218893012 | Rare:100; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr2:218893015-218893289 | Rare:88; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 |