| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:206470349-206470455 | Common:3; Rare:15 | ||||
| chr1:206507349-206507532 | Common:2; Rare:41 | ||||
| chr1:206557340-206557600 | Common:2; Rare:60 | ||||
| chr1:206612428-206612713 | Common:6; Rare:84 | ||||
| chr1:206635302-206635584 | Common:4; Rare:82 | ||||
| chr1:206635868-206636016 | Rare:52 | ||||
| chr1:206684755-206684939 | Rare:60 | ||||
| chr1:207050920-207051145 | Common:1; Rare:104 | ||||
| chr1:207052956-207053263 | Rare:76 | ||||
| chr1:207321588-207321703 | Rare:28 | ||||
| chr1:207751840-207752137 | Common:2; Rare:99 | ||||
| chr1:208244232-208244540 | Common:1; Rare:89 | ||||
| chr1:209784439-209784780 | Common:1; Rare:108 | ||||
| chr1:209827800-209828029 | Common:2; Rare:56 | ||||
| chr1:209938073-209938280 | Common:2; Rare:83; Clinvar (pathogenic):1 |