Variant report
| Variant | rs542080727 |
|---|---|
| Chromosome Location | chr1:102097562-102097563 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:102095600-102098000 | Weak transcription | 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
Copyright © 2015, Bioinformatics Lab, Institute of Psychology, Chinese Academy of Sciences. All Rights Reserved
Feedback
Last update: Aug 31, 2015