| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:151198728-151199128 | Common:4; Rare:148 | ||||
| chr1:151254597-151254801 | Rare:48 | ||||
| chr1:151281235-151281534 | Common:3; Rare:91 | ||||
| chr1:151281832-151282312 | Rare:125 | ||||
| chr1:151327590-151327856 | Common:2; Rare:52 | ||||
| chr1:151346818-151347015 | Rare:57 | ||||
| chr1:151347228-151347569 | Rare:77 | ||||
| chr1:151372652-151372812 | Common:2; Rare:36 | ||||
| chr1:151399385-151399596 | Common:1; Rare:61; Clinvar (pathogenic):1 | ||||
| chr1:151458476-151458766 | Common:5; Rare:119 | ||||
| chr1:151459330-151460150 | Common:4; Rare:235 | ||||
| chr1:151511092-151511438 | Common:4; Rare:77 | ||||
| chr1:151533945-151534345 | Common:2; Rare:167 | ||||
| chr1:151540106-151540373 | Common:1; Rare:83 | ||||
| chr1:151611866-151612226 | Common:3; Rare:84; Clinvar (benign):1 |