| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45522447-45522631 | Common:1; Rare:26 | ||||
| chr1:45550539-45551131 | Common:4; Rare:137 | ||||
| chr1:45583258-45583630 | Common:4; Rare:90 | ||||
| chr1:45583917-45584123 | Rare:80 | ||||
| chr1:45686452-45686858 | Rare:140 | ||||
| chr1:45687023-45687480 | Common:2; Rare:124 | ||||
| chr1:45687522-45687672 | Common:4; Rare:26 | ||||
| chr1:45688017-45688234 | Common:1; Rare:55 | ||||
| chr1:45750403-45750986 | Common:3; Rare:172 | ||||
| chr1:45750998-45751092 | Common:2; Rare:17 | ||||
| chr1:45803376-45803690 | Common:2; Rare:110 | ||||
| chr1:46132149-46132194 | Rare:5 | ||||
| chr1:46198342-46198655 | Common:7; Rare:134; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:46247672-46247898 | Common:2; Rare:43 | ||||
| chr1:46303149-46303745 | Common:3; Rare:177 |