| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45011213-45011379 | Rare:44 | ||||
| chr1:45012005-45012327 | Common:2; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:45012692-45013172 | Common:1; Rare:142 | ||||
| chr1:45014711-45015004 | Common:1; Rare:88; Clinvar (pathogenic):4 | ||||
| chr1:45339933-45340265 | Common:1; Rare:127; Clinvar:13; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr1:45340329-45340588 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:45340933-45341107 | Common:1; Rare:43 | ||||
| chr1:45491120-45491457 | Common:3; Rare:91 | ||||
| chr1:45499941-45500348 | Common:2; Rare:93; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521818-45522089 | Common:1; Rare:101 | ||||
| chr1:45550709-45551154 | Common:3; Rare:106 | ||||
| chr1:45566683-45567097 | Common:3; Rare:112 | ||||
| chr1:45567697-45568197 | Common:2; Rare:146 | ||||
| chr1:45568392-45568568 | Rare:39 | ||||
| chr1:45568970-45569229 | Common:1; Rare:65 |