| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:52142640-52142970 | Rare:114 | ||||
| chr1:52365405-52366660 | Common:26; Rare:935 | ||||
| chr1:52403590-52404060 | Common:3; Rare:189 | ||||
| chr1:52404306-52404706 | Common:7; Rare:590 | ||||
| chr1:52404799-52405224 | Common:1; Rare:193 | ||||
| chr1:52552154-52552554 | Common:1; Rare:91 | ||||
| chr1:52552530-52552850 | Rare:177 | ||||
| chr1:52552870-52553010 | Common:1; Rare:36 | ||||
| chr1:52552941-52553387 | Common:23; Rare:569 | ||||
| chr1:52553320-52553730 | Common:17; Rare:505 | ||||
| chr1:52698012-52698736 | Common:18; Rare:646; Clinvar (pathogenic):4 | ||||
| chr1:52726172-52726572 | Common:22; Rare:345 | ||||
| chr1:52726574-52726994 | Common:2; Rare:187 | ||||
| chr1:52842520-52843526 | Common:56; Rare:1030 | ||||
| chr1:52905068-52905807 | Common:4; Rare:245 |