| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:52365901-52366720 | Common:9; Rare:446 | ||||
| chr1:52404316-52404774 | Common:5; Rare:335 | ||||
| chr1:52553201-52553880 | Common:10; Rare:380 | ||||
| chr1:52697890-52698562 | Common:14; Rare:432; Clinvar (pathogenic):3 | ||||
| chr1:52726440-52726584 | Common:5; Rare:54 | ||||
| chr1:52842466-52842970 | Common:16; Rare:293 | ||||
| chr1:52920944-52921410 | Common:8; Rare:165 | ||||
| chr1:52927079-52927405 | Common:8; Rare:151 | ||||
| chr1:53014720-53015110 | Common:1; Rare:180; Clinvar:1; Clinvar (benign):3 | ||||
| chr1:53196640-53196907 | Common:1; Rare:187; Clinvar:12; Clinvar (benign):2 | ||||
| chr1:53197320-53197770 | Common:2; Rare:84 | ||||
| chr1:53220150-53220553 | Common:1; Rare:317 | ||||
| chr1:53220554-53220828 | Common:6; Rare:300 | ||||
| chr1:53238416-53238803 | Common:6; Rare:272 | ||||
| chr1:53326393-53327063 | Common:6; Rare:161 |