| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45551249-45551302 | Common:1; Rare:8 | ||||
| chr1:45583305-45583636 | Common:3; Rare:82 | ||||
| chr1:45583854-45584114 | Common:1; Rare:97 | ||||
| chr1:45686105-45686165 | Rare:18 | ||||
| chr1:45686451-45686772 | Rare:118 | ||||
| chr1:45687049-45687708 | Common:5; Rare:161 | ||||
| chr1:45688007-45688281 | Common:1; Rare:67 | ||||
| chr1:45688338-45688436 | Common:2; Rare:16 | ||||
| chr1:45750237-45750944 | Common:3; Rare:198 | ||||
| chr1:45750948-45751076 | Common:1; Rare:25 | ||||
| chr1:45803372-45803690 | Common:2; Rare:110 | ||||
| chr1:46131964-46132197 | Rare:60 | ||||
| chr1:46132472-46133027 | Common:4; Rare:176 | ||||
| chr1:46133312-46133605 | Common:1; Rare:70 | ||||
| chr1:46198276-46198630 | Common:7; Rare:144; Clinvar:1; Clinvar (benign):3 |