Variant report

Variant	rs1546671
Chromosome Location	chr11:33984088-33984089
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1518919	1.00[AMR][1000 genomes]
rs1589183	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2056250	1.00[AMR][1000 genomes]
rs2901433	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34073861	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34166865	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35565294	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35743871	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35755947	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4429033	1.00[YRI][hapmap];1.00[AMR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33981400-33985600	Enhancers	K562	blood
2	chr11:33983200-33992400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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

Quick links