| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:52404797-52404859 | Rare:9 | ||||
| chr1:52552646-52552675 | Rare:7 | ||||
| chr1:52552934-52553268 | Common:3; Rare:105 | ||||
| chr1:52553321-52553737 | Common:3; Rare:114 | ||||
| chr1:52602293-52602586 | Common:2; Rare:100 | ||||
| chr1:52602626-52602792 | Common:3; Rare:38 | ||||
| chr1:52697908-52697938 | Common:2; Rare:8 | ||||
| chr1:52698234-52698514 | Common:3; Rare:93; Clinvar (pathogenic):1 | ||||
| chr1:52726344-52726579 | Common:9; Rare:99 | ||||
| chr1:52921624-52921833 | Common:1; Rare:64 | ||||
| chr1:52927185-52927377 | Common:4; Rare:66 | ||||
| chr1:53014765-53015014 | Rare:68 | ||||
| chr1:53061931-53062224 | Common:5; Rare:64 | ||||
| chr1:53062495-53062536 | Rare:5 | ||||
| chr1:53196600-53196935 | Common:1; Rare:115; Clinvar:6; Clinvar (benign):1 |