Variant report
| Variant | rs6696558 |
|---|---|
| Chromosome Location | chr1:220709767-220709768 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:220703400-220724400 | Weak transcription | Aorta | Aorta |
| 2 | chr1:220704600-220710000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 3 | chr1:220706000-220723800 | Weak transcription | Fetal Brain Male | brain |
| 4 | chr1:220706800-220710400 | ZNF genes & repeats | Cortex derived primary cultured neurospheres | brain |
| 5 | chr1:220708800-220718000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 6 | chr1:220709400-220710000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
