Variant report

Variant	rs9885929
Chromosome Location	chr6:50070495-50070496
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs13437462	1.00[YRI][hapmap]
rs9463564	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs9463565	1.00[AMR][1000 genomes]
rs9463568	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9463571	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473715	1.00[AMR][1000 genomes]
rs9473717	1.00[AMR][1000 genomes]
rs9473719	1.00[YRI][hapmap]
rs9473720	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs9473721	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs9473724	1.00[AMR][1000 genomes]
rs9473734	1.00[YRI][hapmap]
rs9473741	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473742	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:50070400-50070600	Enhancers	HSMM	muscle

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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

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