Variant report

Variant	rs7736333
Chromosome Location	chr5:43804591-43804592
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10050559	1.00[EUR][1000 genomes]
rs10051788	1.00[EUR][1000 genomes]
rs10473316	1.00[EUR][1000 genomes]
rs12109668	0.88[YRI][hapmap]
rs13360905	1.00[EUR][1000 genomes]
rs55912106	1.00[EUR][1000 genomes]
rs58908791	1.00[EUR][1000 genomes]
rs6874715	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6897781	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73751786	1.00[EUR][1000 genomes]
rs73751789	1.00[EUR][1000 genomes]
rs73751792	1.00[EUR][1000 genomes]
rs73751797	1.00[EUR][1000 genomes]
rs73753604	1.00[EUR][1000 genomes]
rs7709214	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7718532	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7736896	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9292888	1.00[EUR][1000 genomes]
rs9688104	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3471542	chr5:43665651-43824536	Weak transcription ZNF genes & repeats Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	esv3471543	chr5:43665767-43824443	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
3	esv2830374	chr5:43785548-44341631	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv964768	chr5:43798587-43818512	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43803200-43804800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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