Variant report

Variant	rs9875332
Chromosome Location	chr3:23092445-23092446
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs58607465	0.91[ASN][1000 genomes]
rs58744973	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61686844	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6794571	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73145951	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73145969	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73821133	0.92[ASN][1000 genomes]
rs9845196	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9849300	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9859420	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9870020	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:23089200-23096800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr3:23090600-23103800	Weak transcription	Aorta	Aorta

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