| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:52553055-52553389 | Common:4; Rare:96 | ||||
| chr1:52602346-52602506 | Common:2; Rare:45 | ||||
| chr1:52921529-52921560 | Common:1; Rare:11 | ||||
| chr1:52926962-52927317 | Common:2; Rare:68 | ||||
| chr1:53220336-53220374 | Rare:17 | ||||
| chr1:53220581-53220712 | Common:2; Rare:61 | ||||
| chr1:53238447-53238608 | Common:2; Rare:68 | ||||
| chr1:53945947-53946055 | Common:2; Rare:35 | ||||
| chr1:53946260-53946475 | Rare:78 | ||||
| chr1:53946556-53946655 | Common:1; Rare:25 | ||||
| chr1:54053176-54053687 | Common:6; Rare:168 | ||||
| chr1:54199985-54200259 | Rare:81 | ||||
| chr1:54548101-54548300 | Common:2; Rare:49 | ||||
| chr1:54801289-54801371 | Rare:15 | ||||
| chr1:54887135-54887392 | Common:1; Rare:85; Clinvar:3; Clinvar (benign):1 |