Variant report

Variant	rs9475203
Chromosome Location	chr6:55084161-55084162
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs1354203	1.00[TSI][hapmap]
rs9464206	0.92[AFR][1000 genomes]
rs9464207	1.00[LWK][hapmap];1.00[MKK][hapmap];0.92[AFR][1000 genomes]
rs9464208	0.92[AFR][1000 genomes]
rs9475197	0.92[AFR][1000 genomes]
rs9475198	0.92[AFR][1000 genomes]
rs9475202	0.84[YRI][hapmap];1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016461	chr6:55038131-55129663	Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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