Variant report

Variant	rs9473724
Chromosome Location	chr6:49998471-49998472
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
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[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9463565	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9463568	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9463571	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473715	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473717	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473719	1.00[YRI][hapmap]
rs9473720	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473721	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473734	1.00[YRI][hapmap]
rs9473741	1.00[YRI][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9473742	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9885929	1.00[YRI][hapmap];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933942	chr6:49480550-50004231	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv5295	chr6:49955078-50007710	Enhancers Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:49998000-49998600	Active TSS	K562	blood
2	chr6:49998200-49998800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:49998400-49998600	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr6:49998400-49998600	Active TSS	iPS-18 Cell Line	embryonic stem cell
5	chr6:49998400-49998800	Enhancers	H1 Cell Line	embryonic stem cell
6	chr6:49998400-49998800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr6:49998400-49998800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr6:49998400-49998800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr6:49998400-49998800	Active TSS	HepG2	liver
10	chr6:49998400-49999000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell

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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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