| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:178093581-178093792 | Common:2; Rare:63 | ||||
| chr1:178094382-178094510 | Rare:62 | ||||
| chr1:178512410-178512654 | Common:2; Rare:36 | ||||
| chr1:178512936-178513225 | Rare:76 | ||||
| chr1:178724897-178725359 | Common:12; Rare:146 | ||||
| chr1:178871037-178871148 | Rare:17 | ||||
| chr1:179025756-179026054 | Common:4; Rare:68 | ||||
| chr1:179293648-179293869 | Common:3; Rare:80 | ||||
| chr1:179365649-179365822 | Common:6; Rare:48 | ||||
| chr1:179365929-179366160 | Common:9; Rare:49 | ||||
| chr1:179591517-179591653 | Common:2; Rare:37 | ||||
| chr1:179591704-179592139 | Common:2; Rare:107 | ||||
| chr1:179877766-179877866 | Rare:22 | ||||
| chr1:179881992-179882331 | Common:4; Rare:79 | ||||
| chr1:179882402-179883064 | Common:4; Rare:302; Clinvar:11; Clinvar (benign):5 |