| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:52920731-52921069 | Common:2; Rare:63 | ||||
| chr1:52927219-52927413 | Common:3; Rare:75; Clinvar:2 | ||||
| chr1:52927578-52927721 | Common:2; Rare:30 | ||||
| chr1:53220581-53220691 | Common:1; Rare:51 | ||||
| chr1:53238446-53238687 | Common:2; Rare:91 | ||||
| chr1:53946260-53946387 | Rare:49 | ||||
| chr1:54053000-54053019 | Rare:5 | ||||
| chr1:54053109-54053715 | Common:6; Rare:199 | ||||
| chr1:54199988-54200241 | Rare:68 | ||||
| chr1:54623276-54623427 | Common:1; Rare:55 | ||||
| chr1:54623434-54623547 | Common:1; Rare:26 | ||||
| chr1:54623551-54623601 | Rare:15 | ||||
| chr1:54801169-54801408 | Common:1; Rare:57 | ||||
| chr1:54980352-54980628 | Common:4; Rare:68 | ||||
| chr1:55039212-55039597 | Common:2; Rare:76; Clinvar:3; Clinvar (benign):1 |