Variant report
| Variant | rs6764338 |
|---|---|
| Chromosome Location | chr3:68777779-68777780 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr3:68777200-68778200 | Enhancers | Fetal Heart | heart |
The 2.0 version of rSNPBase
Quick Search:
Input of quick search could be:- dbSNP/dbVar ID: rs12345 /nsv7879
- a single nucleotide as 0-based coordinates: chr1:12345
- chromosomal regions: chr1:12345-34567
what's new
- New variant types
- New dimension of annotation
- New regulatory manner
- More detailed annotation on variant overlapped TFBS
- More extended data
- New search manner
Quick links
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Last update: Aug 31, 2015