| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:44775824-44775977 | Common:2; Rare:66 | ||||
| chr1:44799633-44800013 | Common:6; Rare:131 | ||||
| chr1:44800153-44800479 | Common:3; Rare:130 | ||||
| chr1:44986512-44986764 | Common:4; Rare:93; Clinvar (benign):2 | ||||
| chr1:45012042-45012283 | Common:2; Rare:159; Clinvar:8; Clinvar (benign):2 | ||||
| chr1:45205630-45206200 | Common:2; Rare:313 | ||||
| chr1:45206353-45206473 | Common:1; Rare:43 | ||||
| chr1:45206535-45206850 | Common:2; Rare:165 | ||||
| chr1:45326780-45326949 | Rare:77 | ||||
| chr1:45339927-45340279 | Common:1; Rare:249; Clinvar:23; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr1:45340381-45340586 | Common:2; Rare:95; Clinvar:2 | ||||
| chr1:45491137-45491376 | Common:2; Rare:64 | ||||
| chr1:45500017-45500417 | Common:3; Rare:207; Clinvar:11; Clinvar (pathogenic):9 | ||||
| chr1:45521800-45522089 | Common:2; Rare:210 | ||||
| chr1:45522774-45522929 | Rare:51 |